| SNP | rat gene | human orthologous gene | Disease |
| ENSRNOSNP2717841 | ENSRNOT00000007913 | ENSG00000156113 | Smith-Lemli-Opitz_syndrome_(2)
|
| ENSRNOSNP2717841 | ENSRNOT00000044150 | ENSG00000156113 | Smith-Lemli-Opitz_syndrome_(2)
|
| ENSRNOSNP2717841 | ENSRNOT00000052375 | ENSG00000156113 | Smith-Lemli-Opitz_syndrome_(2)
|
| ENSRNOSNP2717841 | ENSRNOT00000061823 | ENSG00000156113 | Smith-Lemli-Opitz_syndrome_(2)
|
| ENSRNOSNP2717881 | ENSRNOT00000020878 | ENSG00000157168 | Thrombophilia_due_to_elevated_HRG_(1)_(?)
|
| ENSRNOSNP2717966 | ENSRNOT00000021481 | ENSG00000111664 | {Hypertension,_essential,_susceptibility_to},_145500_(3)
|
| ENSRNOSNP2717966 | ENSRNOT00000056039 | ENSG00000111664 | {Hypertension,_essential,_susceptibility_to},_145500_(3)
|
| ENSRNOSNP2717966 | ENSRNOT00000020803 | ENSG00000111664 | {Hypertension,_essential,_susceptibility_to},_145500_(3)
|
| ENSRNOSNP2717966 | ENSRNOT00000041609 | ENSG00000111664 | {Hypertension,_essential,_susceptibility_to},_145500_(3)
|
| ENSRNOSNP2717966 | ENSRNOT00000020785 | ENSG00000111664 | {Hypertension,_essential,_susceptibility_to},_145500_(3)
|
| ENSRNOSNP2717997 | ENSRNOT00000023387 | ENSG00000122194 | Plasminogen_Tochigi_disease_(3)
|
| ENSRNOSNP2717997 | ENSRNOT00000023387 | ENSG00000122194 | Plasminogen_deficiency,_types_I_and_II_(1)
|
| ENSRNOSNP2717997 | ENSRNOT00000023387 | ENSG00000122194 | Thrombophilia,_dysplasminogenemic_(1)
|
| ENSRNOSNP2717997 | ENSRNOT00000023368 | ENSG00000122194 | Plasminogen_Tochigi_disease_(3)
|
| ENSRNOSNP2717997 | ENSRNOT00000023368 | ENSG00000122194 | Plasminogen_deficiency,_types_I_and_II_(1)
|
| ENSRNOSNP2717997 | ENSRNOT00000023368 | ENSG00000122194 | Thrombophilia,_dysplasminogenemic_(1)
|
| ENSRNOSNP2718039 | ENSRNOT00000015491 | ENSG00000065618 | Epidermolysis_bullosa,_generalized_atrophic_benign,_226650_(3)
|
| ENSRNOSNP2718039 | ENSRNOT00000015495 | ENSG00000065618 | Epidermolysis_bullosa,_generalized_atrophic_benign,_226650_(3)
|
| ENSRNOSNP2718039 | ENSRNOT00000016645 | ENSG00000065618 | Epidermolysis_bullosa,_generalized_atrophic_benign,_226650_(3)
|
| ENSRNOSNP2718039 | ENSRNOT00000045074 | ENSG00000065618 | Epidermolysis_bullosa,_generalized_atrophic_benign,_226650_(3)
|
| ENSRNOSNP2718174 | ENSRNOT00000018535 | ENSG00000140937 | Obesity,_severe,_due_to_leptin_deficiency_(3)
|
| ENSRNOSNP2718278 | ENSRNOT00000002717 | ENSG00000180509 | Jervell_and_Lange-Nielsen_syndrome,_220400_(3)
|
| ENSRNOSNP2718531 | ENSRNOT00000013262 | ENSG00000171503 | Glutaricaciduria,_type_IIC_(3)
|
| ENSRNOSNP2718577 | ENSRNOT00000014505 | ENSG00000168878 | Pulmonary_alveolar_proteinosis,_congenital,_265120_(3)
|
| ENSRNOSNP2718577 | ENSRNOT00000016699 | ENSG00000168878 | Pulmonary_alveolar_proteinosis,_congenital,_265120_(3)
|
| ENSRNOSNP2718698 | ENSRNOT00000021390 | ENSG00000160654 | Immunodeficiency_due_to_defect_in_CD3-gamma_(3)
|
| ENSRNOSNP2718698 | ENSRNOT00000021488 | ENSG00000160654 | Immunodeficiency_due_to_defect_in_CD3-gamma_(3)
|
| ENSRNOSNP2718759 | ENSRNOT00000058345 | ENSG00000197919 | Interferon,_alpha,_deficiency_(1)
|
| ENSRNOSNP2718790 | ENSRNOT00000007913 | ENSG00000156113 | Smith-Lemli-Opitz_syndrome_(2)
|
| ENSRNOSNP2718790 | ENSRNOT00000044150 | ENSG00000156113 | Smith-Lemli-Opitz_syndrome_(2)
|
| ENSRNOSNP2718790 | ENSRNOT00000052375 | ENSG00000156113 | Smith-Lemli-Opitz_syndrome_(2)
|
| ENSRNOSNP2718884 | ENSRNOT00000006856 | ENSG00000186868 | Dementia,_frontotemporal,_with_parkinsonism,_601630_(3)
|
| ENSRNOSNP2718884 | ENSRNOT00000006856 | ENSG00000186868 | Parkinsonism-dementia_with_pallidopontonigral_degeneration_(2)
|
| ENSRNOSNP2718884 | ENSRNOT00000006947 | ENSG00000186868 | Dementia,_frontotemporal,_with_parkinsonism,_601630_(3)
|
| ENSRNOSNP2718884 | ENSRNOT00000006947 | ENSG00000186868 | Parkinsonism-dementia_with_pallidopontonigral_degeneration_(2)
|
| ENSRNOSNP2718884 | ENSRNOT00000042984 | ENSG00000186868 | Dementia,_frontotemporal,_with_parkinsonism,_601630_(3)
|
| ENSRNOSNP2718884 | ENSRNOT00000042984 | ENSG00000186868 | Parkinsonism-dementia_with_pallidopontonigral_degeneration_(2)
|
| ENSRNOSNP2718884 | ENSRNOT00000043604 | ENSG00000186868 | Dementia,_frontotemporal,_with_parkinsonism,_601630_(3)
|
| ENSRNOSNP2718884 | ENSRNOT00000043604 | ENSG00000186868 | Parkinsonism-dementia_with_pallidopontonigral_degeneration_(2)
|
| ENSRNOSNP2718884 | ENSRNOT00000045127 | ENSG00000186868 | Dementia,_frontotemporal,_with_parkinsonism,_601630_(3)
|
| ENSRNOSNP2718884 | ENSRNOT00000045127 | ENSG00000186868 | Parkinsonism-dementia_with_pallidopontonigral_degeneration_(2)
|
| ENSRNOSNP2718884 | ENSRNOT00000045134 | ENSG00000186868 | Dementia,_frontotemporal,_with_parkinsonism,_601630_(3)
|
| ENSRNOSNP2718884 | ENSRNOT00000045134 | ENSG00000186868 | Parkinsonism-dementia_with_pallidopontonigral_degeneration_(2)
|
| ENSRNOSNP2718884 | ENSRNOT00000050070 | ENSG00000186868 | Dementia,_frontotemporal,_with_parkinsonism,_601630_(3)
|
| ENSRNOSNP2718884 | ENSRNOT00000050070 | ENSG00000186868 | Parkinsonism-dementia_with_pallidopontonigral_degeneration_(2)
|
| ENSRNOSNP2718985 | ENSRNOT00000023414 | ENSG00000107518 | {Atherosclerosis,_susceptibility_to}_(2)
|
| ENSRNOSNP2719034 | ENSRNOT00000023414 | ENSG00000107518 | {Atherosclerosis,_susceptibility_to}_(2)
|
| ENSRNOSNP2719065 | ENSRNOT00000005016 | ENSG00000174231 | Retinitis_pigmentosa-13_(2)
|
| ENSRNOSNP2719065 | ENSRNOT00000056346 | ENSG00000174231 | Retinitis_pigmentosa-13_(2)
|
| ENSRNOSNP2719136 | ENSRNOT00000023363 | ENSG00000107518 | {Atherosclerosis,_susceptibility_to}_(2)
|
| ENSRNOSNP2719136 | ENSRNOT00000023414 | ENSG00000107518 | {Atherosclerosis,_susceptibility_to}_(2)
|
| ENSRNOSNP2719419 | ENSRNOT00000035247 | ENSG00000121031 | Severe_combined_immunodeficiency,_type_I,_202500_(1)_(?)
|
| ENSRNOSNP2719536 | ENSRNOT00000020775 | ENSG00000196959 | Monocyte_carboxyesterase_deficiency_(1)_(?)
|
| ENSRNOSNP2719540 | ENSRNOT00000025845 | ENSG00000107798 | Cholesteryl_ester_storage_disease_(3)
|
| ENSRNOSNP2719540 | ENSRNOT00000025845 | ENSG00000107798 | Wolman_disease_(3)
|
| ENSRNOSNP2719751 | ENSRNOT00000027367 | ENSG00000124813 | Cleidocranial_dysplasia,_119600_(3)
|
| ENSRNOSNP2719751 | ENSRNOT00000061012 | ENSG00000124813 | Cleidocranial_dysplasia,_119600_(3)
|
| ENSRNOSNP2719751 | ENSRNOT00000061014 | ENSG00000124813 | Cleidocranial_dysplasia,_119600_(3)
|
| ENSRNOSNP2719818 | ENSRNOT00000019197 | ENSG00000075891 | Optic_nerve_coloboma_with_renal_disease,_120330_(3)
|
| ENSRNOSNP2719818 | ENSRNOT00000050076 | ENSG00000075891 | Optic_nerve_coloboma_with_renal_disease,_120330_(3)
|
| ENSRNOSNP2719828 | ENSRNOT00000028701 | ENSG00000124299 | Prolidase_deficiency_(3)
|
| ENSRNOSNP2719828 | ENSRNOT00000028701 | ENSG00000124299 | Prolidase_deficiency_(3)
|
| ENSRNOSNP2719991 | ENSRNOT00000017023 | ENSG00000085276 | 3q21q26_syndrome_(1)
|
| ENSRNOSNP2720044 | ENSRNOT00000020775 | ENSG00000196959 | Monocyte_carboxyesterase_deficiency_(1)_(?)
|
| ENSRNOSNP2720132 | ENSRNOT00000020544 | ENSG00000140374 | Glutaricaciduria,_type_IIA_(1)
|
| ENSRNOSNP2720199 | ENSRNOT00000024065 | ENSG00000175535 | Pancreatic_lipase_deficiency_(1)
|
| ENSRNOSNP2720263 | ENSRNOT00000015750 | ENSG00000053747 | Epidermolysis_bullosa,_junctional,_Herlitz_type_(3)
|
| ENSRNOSNP2720300 | ENSRNOT00000035692 | ENSG00000198947 | Becker_muscular_dystrophy_(3)
|
| ENSRNOSNP2720300 | ENSRNOT00000035692 | ENSG00000198947 | Cardiomyopathy,_dilated,_X-linked_(3)
|
| ENSRNOSNP2720300 | ENSRNOT00000035692 | ENSG00000198947 | Duchenne_muscular_dystrophy_(3)
|
| ENSRNOSNP2720303 | ENSRNOT00000045074 | ENSG00000065618 | Epidermolysis_bullosa,_generalized_atrophic_benign,_226650_(3)
|
| ENSRNOSNP2720330 | ENSRNOT00000000744 | ENSG00000150275 | Usher_syndrome,_type_IF_(2)
|
| ENSRNOSNP2720374 | ENSRNOT00000035252 | ENSG00000162374 | Paraneoplastic_sensory_neuropathy_(1)
|
| ENSRNOSNP2720374 | ENSRNOT00000035262 | ENSG00000162374 | Paraneoplastic_sensory_neuropathy_(1)
|
| ENSRNOSNP2720532 | ENSRNOT00000018449 | ENSG00000113318 | Endometrial_carcinoma_(3)
|
| ENSRNOSNP2720532 | ENSRNOT00000045570 | ENSG00000113318 | Endometrial_carcinoma_(3)
|
| ENSRNOSNP2720550 | ENSRNOT00000034969 | ENSG00000153956 | {Malignant_hyperthermia_susceptibility_3}_(2)
|
| ENSRNOSNP2720550 | ENSRNOT00000042914 | ENSG00000153956 | {Malignant_hyperthermia_susceptibility_3}_(2)
|
| ENSRNOSNP2720550 | ENSRNOT00000043865 | ENSG00000153956 | {Malignant_hyperthermia_susceptibility_3}_(2)
|
| ENSRNOSNP2720680 | ENSRNOT00000002717 | ENSG00000180509 | Jervell_and_Lange-Nielsen_syndrome,_220400_(3)
|
| ENSRNOSNP2720763 | ENSRNOT00000045717 | ENSG00000085662 | Androgen_insensitivity,_several_forms_(3)
|
| ENSRNOSNP2720763 | ENSRNOT00000045717 | ENSG00000085662 | Breast_cancer,_male,_with_Reifenstein_syndrome_(3)
|
| ENSRNOSNP2720763 | ENSRNOT00000045717 | ENSG00000085662 | Perineal_hypospadias_(3)
|
| ENSRNOSNP2720763 | ENSRNOT00000045717 | ENSG00000085662 | Prostate_cancer_(3)
|
| ENSRNOSNP2720763 | ENSRNOT00000045717 | ENSG00000085662 | Spinal_and_bulbar_muscular_atrophy_of_Kennedy,_313200_(3)
|
| ENSRNOSNP2720961 | ENSRNOT00000049101 | ENSG00000113966 | Bardet-Biedl_syndrome_3_(2)
|
| ENSRNOSNP2721082 | ENSRNOT00000007913 | ENSG00000156113 | Smith-Lemli-Opitz_syndrome_(2)
|
| ENSRNOSNP2721082 | ENSRNOT00000044150 | ENSG00000156113 | Smith-Lemli-Opitz_syndrome_(2)
|
| ENSRNOSNP2721082 | ENSRNOT00000052375 | ENSG00000156113 | Smith-Lemli-Opitz_syndrome_(2)
|
| ENSRNOSNP2721082 | ENSRNOT00000061823 | ENSG00000156113 | Smith-Lemli-Opitz_syndrome_(2)
|
| ENSRNOSNP2721136 | ENSRNOT00000015946 | ENSG00000129084 | Thrombophilia_due_to_heparin_cofactor_II_deficiency_(3)
|
| ENSRNOSNP2721330 | ENSRNOT00000055202 | ENSG00000012048 | Breast_cancer-1_(3)
|
| ENSRNOSNP2721330 | ENSRNOT00000055202 | ENSG00000012048 | Ovarian_cancer_(3)
|
| ENSRNOSNP2721330 | ENSRNOT00000028109 | ENSG00000012048 | Breast_cancer-1_(3)
|
| ENSRNOSNP2721330 | ENSRNOT00000028109 | ENSG00000012048 | Ovarian_cancer_(3)
|
| ENSRNOSNP2721506 | ENSRNOT00000045408 | ENSG00000187323 | Colorectal_cancer_(3)
|
| ENSRNOSNP2721528 | ENSRNOT00000003224 | ENSG00000170624 | Muscular_dystrophy,_limb-girdle,_type_2F,_601287_(3)
|
| ENSRNOSNP2721528 | ENSRNOT00000042561 | ENSG00000170624 | Muscular_dystrophy,_limb-girdle,_type_2F,_601287_(3)
|
| ENSRNOSNP2721663 | ENSRNOT00000005015 | ENSG00000054983 | Krabbe_disease_(3)
|
| ENSRNOSNP2721701 | ENSRNOT00000009634 | ENSG00000158125 | Xanthinuria,_type_I_(3)
|
| ENSRNOSNP2721701 | ENSRNOT00000009634 | ENSG00000158125 | Xanthinuria,_type_I_(3)
|
| ENSRNOSNP2721709 | ENSRNOT00000052292 | ENSG00000188536 | Erythremias,_alpha-_(3)
|
| ENSRNOSNP2721709 | ENSRNOT00000052292 | ENSG00000188536 | Heinz_body_anemias,_alpha-_(3)
|
| ENSRNOSNP2721709 | ENSRNOT00000052292 | ENSG00000188536 | Methemoglobinemias,_alpha-_(3)
|
| ENSRNOSNP2721709 | ENSRNOT00000052292 | ENSG00000188536 | Thalassemias,_alpha-_(3)
|
| ENSRNOSNP2721709 | ENSRNOT00000052292 | ENSG00000206172 | Erythremias,_alpha-_(3)
|
| ENSRNOSNP2721709 | ENSRNOT00000052292 | ENSG00000206172 | Heinz_body_anemias,_alpha-_(3)
|
| ENSRNOSNP2721709 | ENSRNOT00000052292 | ENSG00000206172 | Methemoglobinemias,_alpha-_(3)
|
| ENSRNOSNP2721709 | ENSRNOT00000052292 | ENSG00000206172 | Thalassemias,_alpha-_(3)
|
| ENSRNOSNP2721709 | ENSRNOT00000048977 | ENSG00000188536 | Erythremias,_alpha-_(3)
|
| ENSRNOSNP2721709 | ENSRNOT00000048977 | ENSG00000188536 | Heinz_body_anemias,_alpha-_(3)
|
| ENSRNOSNP2721709 | ENSRNOT00000048977 | ENSG00000188536 | Methemoglobinemias,_alpha-_(3)
|
| ENSRNOSNP2721709 | ENSRNOT00000048977 | ENSG00000188536 | Thalassemias,_alpha-_(3)
|
| ENSRNOSNP2721709 | ENSRNOT00000048977 | ENSG00000206172 | Erythremias,_alpha-_(3)
|
| ENSRNOSNP2721709 | ENSRNOT00000048977 | ENSG00000206172 | Heinz_body_anemias,_alpha-_(3)
|
| ENSRNOSNP2721709 | ENSRNOT00000048977 | ENSG00000206172 | Methemoglobinemias,_alpha-_(3)
|
| ENSRNOSNP2721709 | ENSRNOT00000048977 | ENSG00000206172 | Thalassemias,_alpha-_(3)
|
| ENSRNOSNP2721721 | ENSRNOT00000026942 | ENSG00000149925 | Aldolase_A_deficiency_(3)
|
| ENSRNOSNP2721721 | ENSRNOT00000026942 | ENSG00000149925 | Aldolase_A_deficiency_(3)
|
| ENSRNOSNP2722054 | ENSRNOT00000007773 | ENSG00000126233 | Maroteaux-Lamy_syndrome,_several_forms_(3)
|
| ENSRNOSNP2722054 | ENSRNOT00000007923 | ENSG00000126233 | Maroteaux-Lamy_syndrome,_several_forms_(3)
|
| ENSRNOSNP2722244 | ENSRNOT00000044279 | ENSG00000145012 | Lipoma_(1)
|
| ENSRNOSNP2722244 | ENSRNOT00000050389 | ENSG00000145012 | Lipoma_(1)
|
| ENSRNOSNP2722416 | ENSRNOT00000048880 | ENSG00000067715 | Sarcoma,_synovial_(1)
|
| ENSRNOSNP1415009 | ENSRNOT00000012928 | ENSG00000102805 | Ceroid-lipofuscinosis,_neuronal-5,_variant_late_infantile_(3)
|
| ENSRNOSNP1415014 | ENSRNOT00000012928 | ENSG00000102805 | Ceroid-lipofuscinosis,_neuronal-5,_variant_late_infantile_(3)
|
| ENSRNOSNP1415015 | ENSRNOT00000012928 | ENSG00000102805 | Ceroid-lipofuscinosis,_neuronal-5,_variant_late_infantile_(3)
|
| ENSRNOSNP2722615 | ENSRNOT00000004716 | ENSG00000163554 | Elliptocytosis-2_(3)
|
| ENSRNOSNP2722615 | ENSRNOT00000004716 | ENSG00000163554 | Pyropoikilocytosis_(3)
|
| ENSRNOSNP2722615 | ENSRNOT00000004716 | ENSG00000163554 | Spherocytosis,_recessive_(3)
|
| ENSRNOSNP2722615 | ENSRNOT00000043311 | ENSG00000163554 | Elliptocytosis-2_(3)
|
| ENSRNOSNP2722615 | ENSRNOT00000043311 | ENSG00000163554 | Pyropoikilocytosis_(3)
|
| ENSRNOSNP2722615 | ENSRNOT00000043311 | ENSG00000163554 | Spherocytosis,_recessive_(3)
|
| ENSRNOSNP2722783 | ENSRNOT00000032388 | ENSG00000183691 | Symphalangism,_proximal_(2)
|
| ENSRNOSNP2722830 | ENSRNOT00000024973 | ENSG00000072778 | VLCAD_deficiency_(3)
|
| ENSRNOSNP2722830 | ENSRNOT00000025211 | ENSG00000072778 | VLCAD_deficiency_(3)
|
| ENSRNOSNP2722830 | ENSRNOT00000056796 | ENSG00000072778 | VLCAD_deficiency_(3)
|
| ENSRNOSNP2723074 | ENSRNOT00000037567 | ENSG00000197535 | Griscelli_disease,_214450_(3)
|
| ENSRNOSNP2723074 | ENSRNOT00000037590 | ENSG00000197535 | Griscelli_disease,_214450_(3)
|
| ENSRNOSNP2723119 | ENSRNOT00000004511 | ENSG00000161021 | Leukotriene_C4_synthase_deficiency_(1)
|
| ENSRNOSNP2723119 | ENSRNOT00000041770 | ENSG00000161021 | Leukotriene_C4_synthase_deficiency_(1)
|
| ENSRNOSNP2723119 | ENSRNOT00000049942 | ENSG00000161021 | Leukotriene_C4_synthase_deficiency_(1)
|
| ENSRNOSNP2723119 | ENSRNOT00000004361 | ENSG00000161021 | Leukotriene_C4_synthase_deficiency_(1)
|
| ENSRNOSNP2723129 | ENSRNOT00000048880 | ENSG00000067715 | Sarcoma,_synovial_(1)
|
| ENSRNOSNP2723131 | ENSRNOT00000059390 | ENSG00000182578 | Myeloid_malignancy,_predisposition_to_(3)
|
| ENSRNOSNP2723131 | ENSRNOT00000024883 | ENSG00000182578 | Myeloid_malignancy,_predisposition_to_(3)
|
| ENSRNOSNP2723131 | ENSRNOT00000049357 | ENSG00000182578 | Myeloid_malignancy,_predisposition_to_(3)
|
| ENSRNOSNP2723131 | ENSRNOT00000059391 | ENSG00000182578 | Myeloid_malignancy,_predisposition_to_(3)
|
| ENSRNOSNP2723291 | ENSRNOT00000047725 | ENSG00000135636 | Miyoshi_myopathy,_254130_(2)
|
| ENSRNOSNP2723291 | ENSRNOT00000047725 | ENSG00000135636 | Muscular_dystrophy,_limb-girdle,_type_2B_(2)
|
| ENSRNOSNP2723291 | ENSRNOT00000051257 | ENSG00000135636 | Miyoshi_myopathy,_254130_(2)
|
| ENSRNOSNP2723291 | ENSRNOT00000051257 | ENSG00000135636 | Muscular_dystrophy,_limb-girdle,_type_2B_(2)
|
| ENSRNOSNP2723376 | ENSRNOT00000026098 | ENSG00000169252 | {Asthma,_nocturnal,_susceptibility_to}_(3)
|
| ENSRNOSNP2723376 | ENSRNOT00000026098 | ENSG00000169252 | {Obesity,_susceptibility_to}_(3)
|
| ENSRNOSNP2723397 | ENSRNOT00000044279 | ENSG00000145012 | Lipoma_(1)
|
| ENSRNOSNP2723397 | ENSRNOT00000050389 | ENSG00000145012 | Lipoma_(1)
|
| ENSRNOSNP2723467 | ENSRNOT00000017333 | ENSG00000000971 | Factor_H_deficiency_(1)
|
| ENSRNOSNP2723467 | ENSRNOT00000017333 | ENSG00000000971 | Hemolytic-uremic_syndrome,_235400_(3)
|
| ENSRNOSNP2723467 | ENSRNOT00000017333 | ENSG00000000971 | Membroproliferative_glomerulonephritis_(1)
|
| ENSRNOSNP2723467 | ENSRNOT00000017749 | ENSG00000000971 | Factor_H_deficiency_(1)
|
| ENSRNOSNP2723467 | ENSRNOT00000017749 | ENSG00000000971 | Hemolytic-uremic_syndrome,_235400_(3)
|
| ENSRNOSNP2723467 | ENSRNOT00000017749 | ENSG00000000971 | Membroproliferative_glomerulonephritis_(1)
|
| ENSRNOSNP2723467 | ENSRNOT00000060111 | ENSG00000000971 | Factor_H_deficiency_(1)
|
| ENSRNOSNP2723467 | ENSRNOT00000060111 | ENSG00000000971 | Hemolytic-uremic_syndrome,_235400_(3)
|
| ENSRNOSNP2723467 | ENSRNOT00000060111 | ENSG00000000971 | Membroproliferative_glomerulonephritis_(1)
|
| ENSRNOSNP2723724 | ENSRNOT00000027871 | ENSG00000053918 | Jervell_and_Lange-Nielsen_syndrome,_220400_(3)
|
| ENSRNOSNP2723724 | ENSRNOT00000027871 | ENSG00000053918 | Long_QT_syndrome-1_(3)
|
| ENSRNOSNP2723724 | ENSRNOT00000027875 | ENSG00000053918 | Jervell_and_Lange-Nielsen_syndrome,_220400_(3)
|
| ENSRNOSNP2723724 | ENSRNOT00000027875 | ENSG00000053918 | Long_QT_syndrome-1_(3)
|
| ENSRNOSNP2723795 | ENSRNOT00000027367 | ENSG00000124813 | Cleidocranial_dysplasia,_119600_(3)
|
| ENSRNOSNP2723795 | ENSRNOT00000061012 | ENSG00000124813 | Cleidocranial_dysplasia,_119600_(3)
|
| ENSRNOSNP2723795 | ENSRNOT00000061013 | ENSG00000124813 | Cleidocranial_dysplasia,_119600_(3)
|
| ENSRNOSNP2723795 | ENSRNOT00000061014 | ENSG00000124813 | Cleidocranial_dysplasia,_119600_(3)
|
| ENSRNOSNP2723835 | ENSRNOT00000027995 | ENSG00000142046 | Maple_syrup_urine_disease,_type_Ia_(3)
|
| ENSRNOSNP2723835 | ENSRNOT00000028026 | ENSG00000142046 | Maple_syrup_urine_disease,_type_Ia_(3)
|
| ENSRNOSNP2723863 | ENSRNOT00000020272 | ENSG00000106688 | Dicarboxylicaminoaciduria,_222730_(1)_(?)
|
| ENSRNOSNP2723865 | ENSRNOT00000018202 | ENSG00000109323 | Mannosidosis,_beta-_(3)
|
| ENSRNOSNP2723877 | ENSRNOT00000040052 | ENSG00000107611 | Vitamin_B12,_selective_intestinal_malabsorption_of_(2)
|
| ENSRNOSNP2723971 | ENSRNOT00000047982 | ENSG00000185345 | Parkinson_disease,_juvenile,_type_2,_600116_(3)
|
| ENSRNOSNP2723971 | ENSRNOT00000049023 | ENSG00000185345 | Parkinson_disease,_juvenile,_type_2,_600116_(3)
|
| ENSRNOSNP2723971 | ENSRNOT00000050014 | ENSG00000185345 | Parkinson_disease,_juvenile,_type_2,_600116_(3)
|
| ENSRNOSNP2724046 | ENSRNOT00000047982 | ENSG00000185345 | Parkinson_disease,_juvenile,_type_2,_600116_(3)
|
| ENSRNOSNP2724046 | ENSRNOT00000049023 | ENSG00000185345 | Parkinson_disease,_juvenile,_type_2,_600116_(3)
|
| ENSRNOSNP2724046 | ENSRNOT00000050014 | ENSG00000185345 | Parkinson_disease,_juvenile,_type_2,_600116_(3)
|
| ENSRNOSNP2724110 | ENSRNOT00000024704 | ENSG00000182578 | Myeloid_malignancy,_predisposition_to_(3)
|
| ENSRNOSNP2724110 | ENSRNOT00000024883 | ENSG00000182578 | Myeloid_malignancy,_predisposition_to_(3)
|
| ENSRNOSNP2724110 | ENSRNOT00000049357 | ENSG00000182578 | Myeloid_malignancy,_predisposition_to_(3)
|
| ENSRNOSNP2724110 | ENSRNOT00000059391 | ENSG00000182578 | Myeloid_malignancy,_predisposition_to_(3)
|
| ENSRNOSNP2724165 | ENSRNOT00000060760 | ENSG00000170927 | Polycystic_kidney_disease,_autosomal_recessive_(2)
|
| ENSRNOSNP2724387 | ENSRNOT00000012474 | ENSG00000119899 | Salla_disease_(2)
|
| ENSRNOSNP2724409 | ENSRNOT00000003224 | ENSG00000170624 | Muscular_dystrophy,_limb-girdle,_type_2F,_601287_(3)
|
| ENSRNOSNP2724409 | ENSRNOT00000042561 | ENSG00000170624 | Muscular_dystrophy,_limb-girdle,_type_2F,_601287_(3)
|
| ENSRNOSNP2724425 | ENSRNOT00000023152 | ENSG00000135929 | Cerebrotendinous_xanthomatosis_(3)
|
| ENSRNOSNP2724621 | ENSRNOT00000012161 | ENSG00000151348 | Exostoses,_multiple,_type_2_(3)
|
| ENSRNOSNP2724669 | ENSRNOT00000005015 | ENSG00000054983 | Krabbe_disease_(3)
|
| ENSRNOSNP2724859 | ENSRNOT00000015065 | ENSG00000197299 | Bloom_syndrome_(3)
|
| ENSRNOSNP2724945 | ENSRNOT00000016205 | ENSG00000139631 | Corneal_dystrophy,_Avellino_type_(3)
|
| ENSRNOSNP2724945 | ENSRNOT00000016205 | ENSG00000139631 | Corneal_dystrophy,_Groenouw_type_I,_121900_(3)
|
| ENSRNOSNP2724945 | ENSRNOT00000016205 | ENSG00000139631 | Corneal_dystrophy,_lattice_type_I,_122200_(3)
|
| ENSRNOSNP2724945 | ENSRNOT00000016205 | ENSG00000139631 | Reis-Bucklers_corneal_dystrophy_(3)
|
| ENSRNOSNP2725007 | ENSRNOT00000000537 | ENSG00000204248 | Deafness,_autosomal_dominant_13_(2)
|
| ENSRNOSNP2725007 | ENSRNOT00000000537 | ENSG00000204248 | OSMED_syndrome,_215150_(3)
|
| ENSRNOSNP2725007 | ENSRNOT00000000537 | ENSG00000204248 | Stickler_syndrome,_type_II,_184840_(3)
|
| ENSRNOSNP2725007 | ENSRNOT00000040193 | ENSG00000204248 | Deafness,_autosomal_dominant_13_(2)
|
| ENSRNOSNP2725007 | ENSRNOT00000040193 | ENSG00000204248 | OSMED_syndrome,_215150_(3)
|
| ENSRNOSNP2725007 | ENSRNOT00000040193 | ENSG00000204248 | Stickler_syndrome,_type_II,_184840_(3)
|
| ENSRNOSNP2725007 | ENSRNOT00000041150 | ENSG00000204248 | Deafness,_autosomal_dominant_13_(2)
|
| ENSRNOSNP2725007 | ENSRNOT00000041150 | ENSG00000204248 | OSMED_syndrome,_215150_(3)
|
| ENSRNOSNP2725007 | ENSRNOT00000041150 | ENSG00000204248 | Stickler_syndrome,_type_II,_184840_(3)
|
| ENSRNOSNP2725007 | ENSRNOT00000043309 | ENSG00000204248 | Deafness,_autosomal_dominant_13_(2)
|
| ENSRNOSNP2725007 | ENSRNOT00000043309 | ENSG00000204248 | OSMED_syndrome,_215150_(3)
|
| ENSRNOSNP2725007 | ENSRNOT00000043309 | ENSG00000204248 | Stickler_syndrome,_type_II,_184840_(3)
|
| ENSRNOSNP2725007 | ENSRNOT00000045533 | ENSG00000204248 | Deafness,_autosomal_dominant_13_(2)
|
| ENSRNOSNP2725007 | ENSRNOT00000045533 | ENSG00000204248 | OSMED_syndrome,_215150_(3)
|
| ENSRNOSNP2725007 | ENSRNOT00000045533 | ENSG00000204248 | Stickler_syndrome,_type_II,_184840_(3)
|
| ENSRNOSNP2725007 | ENSRNOT00000045620 | ENSG00000204248 | Deafness,_autosomal_dominant_13_(2)
|
| ENSRNOSNP2725007 | ENSRNOT00000045620 | ENSG00000204248 | OSMED_syndrome,_215150_(3)
|
| ENSRNOSNP2725007 | ENSRNOT00000045620 | ENSG00000204248 | Stickler_syndrome,_type_II,_184840_(3)
|
| ENSRNOSNP2725007 | ENSRNOT00000047081 | ENSG00000204248 | Deafness,_autosomal_dominant_13_(2)
|
| ENSRNOSNP2725007 | ENSRNOT00000047081 | ENSG00000204248 | OSMED_syndrome,_215150_(3)
|
| ENSRNOSNP2725007 | ENSRNOT00000047081 | ENSG00000204248 | Stickler_syndrome,_type_II,_184840_(3)
|
| ENSRNOSNP2725007 | ENSRNOT00000048519 | ENSG00000204248 | Deafness,_autosomal_dominant_13_(2)
|
| ENSRNOSNP2725007 | ENSRNOT00000048519 | ENSG00000204248 | OSMED_syndrome,_215150_(3)
|
| ENSRNOSNP2725007 | ENSRNOT00000048519 | ENSG00000204248 | Stickler_syndrome,_type_II,_184840_(3)
|
| ENSRNOSNP2725058 | ENSRNOT00000006856 | ENSG00000186868 | Dementia,_frontotemporal,_with_parkinsonism,_601630_(3)
|
| ENSRNOSNP2725058 | ENSRNOT00000006856 | ENSG00000186868 | Parkinsonism-dementia_with_pallidopontonigral_degeneration_(2)
|
| ENSRNOSNP2725058 | ENSRNOT00000006947 | ENSG00000186868 | Dementia,_frontotemporal,_with_parkinsonism,_601630_(3)
|
| ENSRNOSNP2725058 | ENSRNOT00000006947 | ENSG00000186868 | Parkinsonism-dementia_with_pallidopontonigral_degeneration_(2)
|
| ENSRNOSNP2725058 | ENSRNOT00000042984 | ENSG00000186868 | Dementia,_frontotemporal,_with_parkinsonism,_601630_(3)
|
| ENSRNOSNP2725058 | ENSRNOT00000042984 | ENSG00000186868 | Parkinsonism-dementia_with_pallidopontonigral_degeneration_(2)
|
| ENSRNOSNP2725058 | ENSRNOT00000043604 | ENSG00000186868 | Dementia,_frontotemporal,_with_parkinsonism,_601630_(3)
|
| ENSRNOSNP2725058 | ENSRNOT00000043604 | ENSG00000186868 | Parkinsonism-dementia_with_pallidopontonigral_degeneration_(2)
|
| ENSRNOSNP2725058 | ENSRNOT00000045127 | ENSG00000186868 | Dementia,_frontotemporal,_with_parkinsonism,_601630_(3)
|
| ENSRNOSNP2725058 | ENSRNOT00000045127 | ENSG00000186868 | Parkinsonism-dementia_with_pallidopontonigral_degeneration_(2)
|
| ENSRNOSNP2725058 | ENSRNOT00000045134 | ENSG00000186868 | Dementia,_frontotemporal,_with_parkinsonism,_601630_(3)
|
| ENSRNOSNP2725058 | ENSRNOT00000045134 | ENSG00000186868 | Parkinsonism-dementia_with_pallidopontonigral_degeneration_(2)
|
| ENSRNOSNP2725058 | ENSRNOT00000050070 | ENSG00000186868 | Dementia,_frontotemporal,_with_parkinsonism,_601630_(3)
|
| ENSRNOSNP2725058 | ENSRNOT00000050070 | ENSG00000186868 | Parkinsonism-dementia_with_pallidopontonigral_degeneration_(2)
|
| ENSRNOSNP2725083 | ENSRNOT00000019498 | ENSG00000104044 | Albinism,_ocular,_autosomal_recessive_(3)
|
| ENSRNOSNP2725083 | ENSRNOT00000019498 | ENSG00000104044 | Albinism,_oculocutaneous,_type_II_(3)
|
| ENSRNOSNP2725097 | ENSRNOT00000014178 | ENSG00000144891 | Ataxia-telangiectasia_(3)
|
| ENSRNOSNP2725097 | ENSRNOT00000014178 | ENSG00000144891 | B-cell_non-Hodgkin_lymphoma,_sporadic_(3)
|
| ENSRNOSNP2725097 | ENSRNOT00000014178 | ENSG00000144891 | Hypertension,_essential,_145500_(3)
|
| ENSRNOSNP2725097 | ENSRNOT00000014178 | ENSG00000144891 | T-cell_prolymphocytic_leukemia,_sporadic_(3)
|
| ENSRNOSNP2725100 | ENSRNOT00000020192 | ENSG00000063854 | [Glyoxalase_II_deficiency]_(1)
|
| ENSRNOSNP2725158 | ENSRNOT00000023414 | ENSG00000107518 | {Atherosclerosis,_susceptibility_to}_(2)
|
| ENSRNOSNP2725164 | ENSRNOT00000041758 | ENSG00000113889 | [Kininogen_deficiency]_(3)
|
| ENSRNOSNP2725164 | ENSRNOT00000044205 | ENSG00000113889 | [Kininogen_deficiency]_(3)
|
| ENSRNOSNP2725164 | ENSRNOT00000048158 | ENSG00000113889 | [Kininogen_deficiency]_(3)
|
| ENSRNOSNP2725164 | ENSRNOT00000051477 | ENSG00000113889 | [Kininogen_deficiency]_(3)
|
| ENSRNOSNP2725261 | ENSRNOT00000045408 | ENSG00000187323 | Colorectal_cancer_(3)
|
| ENSRNOSNP2725331 | ENSRNOT00000028188 | ENSG00000167986 | Xeroderma_pigmentosum,_group_E,_subtype_2_(1)
|
| ENSRNOSNP2725422 | ENSRNOT00000011369 | ENSG00000092529 | Muscular_dystrophy,_limb-girdle,_type_2A,_253600_(3)
|
| ENSRNOSNP2725422 | ENSRNOT00000011761 | ENSG00000092529 | Muscular_dystrophy,_limb-girdle,_type_2A,_253600_(3)
|
| ENSRNOSNP2725422 | ENSRNOT00000046044 | ENSG00000092529 | Muscular_dystrophy,_limb-girdle,_type_2A,_253600_(3)
|
| ENSRNOSNP2725422 | ENSRNOT00000050361 | ENSG00000092529 | Muscular_dystrophy,_limb-girdle,_type_2A,_253600_(3)
|
| ENSRNOSNP2725502 | ENSRNOT00000011369 | ENSG00000092529 | Muscular_dystrophy,_limb-girdle,_type_2A,_253600_(3)
|
| ENSRNOSNP2725502 | ENSRNOT00000011761 | ENSG00000092529 | Muscular_dystrophy,_limb-girdle,_type_2A,_253600_(3)
|
| ENSRNOSNP2725502 | ENSRNOT00000046044 | ENSG00000092529 | Muscular_dystrophy,_limb-girdle,_type_2A,_253600_(3)
|
| ENSRNOSNP2725502 | ENSRNOT00000050361 | ENSG00000092529 | Muscular_dystrophy,_limb-girdle,_type_2A,_253600_(3)
|
| ENSRNOSNP2725560 | ENSRNOT00000043663 | ENSG00000090402 | Sucrose_intolerance_(3)
|
| ENSRNOSNP2725560 | ENSRNOT00000042844 | ENSG00000090402 | Sucrose_intolerance_(3)
|
| ENSRNOSNP2725560 | ENSRNOT00000046681 | ENSG00000090402 | Sucrose_intolerance_(3)
|
| ENSRNOSNP2725836 | ENSRNOT00000004908 | ENSG00000115850 | Lactase_deficiency,_adult,_223100_(1)_(?)
|
| ENSRNOSNP2725836 | ENSRNOT00000004908 | ENSG00000115850 | Lactase_deficiency,_congenital_(1)_(?)
|
| ENSRNOSNP2725872 | ENSRNOT00000004983 | ENSG00000047597 | McLeod_phenotype_(3)
|
| ENSRNOSNP2725872 | ENSRNOT00000040359 | ENSG00000047597 | McLeod_phenotype_(3)
|
| ENSRNOSNP2725872 | ENSRNOT00000051135 | ENSG00000047597 | McLeod_phenotype_(3)
|
| ENSRNOSNP2726032 | ENSRNOT00000039375 | ENSG00000021574 | Spastic_paraplegia-4_(3)
|
| ENSRNOSNP2726154 | ENSRNOT00000019498 | ENSG00000104044 | Albinism,_ocular,_autosomal_recessive_(3)
|
| ENSRNOSNP2726154 | ENSRNOT00000019498 | ENSG00000104044 | Albinism,_oculocutaneous,_type_II_(3)
|
| ENSRNOSNP2726154 | ENSRNOT00000032326 | ENSG00000104044 | Albinism,_ocular,_autosomal_recessive_(3)
|
| ENSRNOSNP2726154 | ENSRNOT00000032326 | ENSG00000104044 | Albinism,_oculocutaneous,_type_II_(3)
|
| ENSRNOSNP2726171 | ENSRNOT00000026556 | ENSG00000134242 | Lymphoproliferative_syndrome,_X-linked_(2)
|
| ENSRNOSNP2726347 | ENSRNOT00000050555 | ENSG00000149311 | Ataxia-telangiectasia_(3)
|
| ENSRNOSNP2726347 | ENSRNOT00000050555 | ENSG00000149311 | B-cell_non-Hodgkin_lymphoma,_sporadic_(3)
|
| ENSRNOSNP2726347 | ENSRNOT00000050555 | ENSG00000149311 | T-cell_prolymphocytic_leukemia,_sporadic_(3)
|
| ENSRNOSNP2726526 | ENSRNOT00000047072 | ENSG00000104447 | Trichorhinophalangeal_syndrome,_type_I_(2)
|
| ENSRNOSNP2726526 | ENSRNOT00000050088 | ENSG00000104447 | Trichorhinophalangeal_syndrome,_type_I_(2)
|
| ENSRNOSNP2726526 | ENSRNOT00000050774 | ENSG00000104447 | Trichorhinophalangeal_syndrome,_type_I_(2)
|
| ENSRNOSNP2726538 | ENSRNOT00000014909 | ENSG00000080618 | Carboxypeptidase_B_deficiency_(1)
|
| ENSRNOSNP2726678 | ENSRNOT00000004511 | ENSG00000161021 | Leukotriene_C4_synthase_deficiency_(1)
|
| ENSRNOSNP2726678 | ENSRNOT00000041770 | ENSG00000161021 | Leukotriene_C4_synthase_deficiency_(1)
|
| ENSRNOSNP2726678 | ENSRNOT00000049942 | ENSG00000161021 | Leukotriene_C4_synthase_deficiency_(1)
|
| ENSRNOSNP2726678 | ENSRNOT00000004361 | ENSG00000161021 | Leukotriene_C4_synthase_deficiency_(1)
|
| ENSRNOSNP2726719 | ENSRNOT00000012342 | ENSG00000179163 | Fucosidosis_(3)
|
| ENSRNOSNP2726719 | ENSRNOT00000012455 | ENSG00000179163 | Fucosidosis_(3)
|
| ENSRNOSNP2726771 | ENSRNOT00000026705 | ENSG00000160789 | Cardiomyopathy,_dilated,_1A_(2)
|
| ENSRNOSNP2726771 | ENSRNOT00000026917 | ENSG00000160789 | Cardiomyopathy,_dilated,_1A_(2)
|
| ENSRNOSNP2726771 | ENSRNOT00000041875 | ENSG00000160789 | Cardiomyopathy,_dilated,_1A_(2)
|
| ENSRNOSNP2726771 | ENSRNOT00000026876 | ENSG00000160789 | Cardiomyopathy,_dilated,_1A_(2)
|
| ENSRNOSNP2726868 | ENSRNOT00000047982 | ENSG00000185345 | Parkinson_disease,_juvenile,_type_2,_600116_(3)
|
| ENSRNOSNP2726868 | ENSRNOT00000049023 | ENSG00000185345 | Parkinson_disease,_juvenile,_type_2,_600116_(3)
|
| ENSRNOSNP2726868 | ENSRNOT00000050014 | ENSG00000185345 | Parkinson_disease,_juvenile,_type_2,_600116_(3)
|
| ENSRNOSNP2727006 | ENSRNOT00000038222 | ENSG00000146070 | Lissencephaly-1_(3)
|
| ENSRNOSNP2727034 | ENSRNOT00000041142 | ENSG00000179295 | Cardiofaciocutaneous_syndrome,_115150_(2)
|
| ENSRNOSNP2727034 | ENSRNOT00000041142 | ENSG00000179295 | Noonan_syndrome-1_(2)
|
| ENSRNOSNP2727034 | ENSRNOT00000046323 | ENSG00000179295 | Cardiofaciocutaneous_syndrome,_115150_(2)
|
| ENSRNOSNP2727034 | ENSRNOT00000046323 | ENSG00000179295 | Noonan_syndrome-1_(2)
|
| ENSRNOSNP2727082 | ENSRNOT00000001738 | ENSG00000174437 | Darier_disease_(keratosis_follicularis)_(2)
|
| ENSRNOSNP2727082 | ENSRNOT00000024347 | ENSG00000174437 | Darier_disease_(keratosis_follicularis)_(2)
|
| ENSRNOSNP2727085 | ENSRNOT00000004505 | ENSG00000158813 | Anhidrotic_ectodermal_dysplasia_(2)
|
| ENSRNOSNP2727085 | ENSRNOT00000004505 | ENSG00000158813 | Ectodermal_dysplasia,_hidrotic_(2)
|
| ENSRNOSNP2727158 | ENSRNOT00000014909 | ENSG00000080618 | Carboxypeptidase_B_deficiency_(1)
|
| ENSRNOSNP2727158 | ENSRNOT00000058266 | ENSG00000080618 | Carboxypeptidase_B_deficiency_(1)
|
| ENSRNOSNP2727185 | ENSRNOT00000013800 | ENSG00000055118 | Long_QT_syndrome-2_(3)
|
| ENSRNOSNP2727185 | ENSRNOT00000051379 | ENSG00000055118 | Long_QT_syndrome-2_(3)
|
| ENSRNOSNP2727342 | ENSRNOT00000010659 | ENSG00000166147 | Ectopia_lentis,_?isolated_(3)
|
| ENSRNOSNP2727342 | ENSRNOT00000010659 | ENSG00000166147 | Marfan_syndrome,_154700_(3)
|
| ENSRNOSNP2727342 | ENSRNOT00000010659 | ENSG00000166147 | Shprintzen-Goldberg_syndrome,_182212_(3)
|
| ENSRNOSNP2727342 | ENSRNOT00000056022 | ENSG00000166147 | Ectopia_lentis,_?isolated_(3)
|
| ENSRNOSNP2727342 | ENSRNOT00000056022 | ENSG00000166147 | Marfan_syndrome,_154700_(3)
|
| ENSRNOSNP2727342 | ENSRNOT00000056022 | ENSG00000166147 | Shprintzen-Goldberg_syndrome,_182212_(3)
|
| ENSRNOSNP2727403 | ENSRNOT00000007079 | ENSG00000005339 | Colorblindness,_protan_(3)
|
| ENSRNOSNP2727403 | ENSRNOT00000007079 | ENSG00000005339 | Rett_syndrome_(2)_(?)
|
| ENSRNOSNP2727403 | ENSRNOT00000007079 | ENSG00000005339 | Rothmund-Thomson_syndrome_(2)_(?)
|
| ENSRNOSNP2727403 | ENSRNOT00000007079 | ENSG00000005339 | Rubenstein-Taybi_syndrome,_180849_(3)
|
| ENSRNOSNP2727403 | ENSRNOT00000049944 | ENSG00000005339 | Colorblindness,_protan_(3)
|
| ENSRNOSNP2727403 | ENSRNOT00000049944 | ENSG00000005339 | Rett_syndrome_(2)_(?)
|
| ENSRNOSNP2727403 | ENSRNOT00000049944 | ENSG00000005339 | Rothmund-Thomson_syndrome_(2)_(?)
|
| ENSRNOSNP2727403 | ENSRNOT00000049944 | ENSG00000005339 | Rubenstein-Taybi_syndrome,_180849_(3)
|
| ENSRNOSNP2727464 | ENSRNOT00000054730 | ENSG00000108242 | Mephenytoin_poor_metabolizer_(3)
|
| ENSRNOSNP2727464 | ENSRNOT00000054730 | ENSG00000138109 | Tolbutamide_poor_metabolizer_(3)
|
| ENSRNOSNP2727464 | ENSRNOT00000054730 | ENSG00000165841 | Mephenytoin_poor_metabolizer_(3)
|
| ENSRNOSNP2727464 | ENSRNOT00000054731 | ENSG00000108242 | Mephenytoin_poor_metabolizer_(3)
|
| ENSRNOSNP2727464 | ENSRNOT00000054731 | ENSG00000138109 | Tolbutamide_poor_metabolizer_(3)
|
| ENSRNOSNP2727464 | ENSRNOT00000054731 | ENSG00000165841 | Mephenytoin_poor_metabolizer_(3)
|
| ENSRNOSNP1437449 | ENSRNOT00000015561 | ENSG00000154122 | Chondrocalcinosis_with_early-onset_osteoarthritis_(2)
|
| ENSRNOSNP2727531 | ENSRNOT00000018449 | ENSG00000113318 | Endometrial_carcinoma_(3)
|
| ENSRNOSNP2727531 | ENSRNOT00000045570 | ENSG00000113318 | Endometrial_carcinoma_(3)
|
| ENSRNOSNP2727564 | ENSRNOT00000016963 | ENSG00000127688 | Giant_axonal_neuropathy-1_(2)
|
| ENSRNOSNP2727714 | ENSRNOT00000004511 | ENSG00000161021 | Leukotriene_C4_synthase_deficiency_(1)
|
| ENSRNOSNP2727714 | ENSRNOT00000041770 | ENSG00000161021 | Leukotriene_C4_synthase_deficiency_(1)
|
| ENSRNOSNP2727714 | ENSRNOT00000049942 | ENSG00000161021 | Leukotriene_C4_synthase_deficiency_(1)
|
| ENSRNOSNP2727714 | ENSRNOT00000004361 | ENSG00000161021 | Leukotriene_C4_synthase_deficiency_(1)
|
| ENSRNOSNP2727762 | ENSRNOT00000020878 | ENSG00000157168 | Thrombophilia_due_to_elevated_HRG_(1)_(?)
|
| ENSRNOSNP2728034 | ENSRNOT00000021786 | ENSG00000162688 | Glycogen_storage_disease_IIIa_(1)
|
| ENSRNOSNP2728034 | ENSRNOT00000021786 | ENSG00000162688 | Glycogen_storage_disease_IIIb_(3)
|
| ENSRNOSNP2728034 | ENSRNOT00000055735 | ENSG00000162688 | Glycogen_storage_disease_IIIa_(1)
|
| ENSRNOSNP2728034 | ENSRNOT00000055735 | ENSG00000162688 | Glycogen_storage_disease_IIIb_(3)
|
| ENSRNOSNP2728034 | ENSRNOT00000021988 | ENSG00000162688 | Glycogen_storage_disease_IIIa_(1)
|
| ENSRNOSNP2728034 | ENSRNOT00000021988 | ENSG00000162688 | Glycogen_storage_disease_IIIb_(3)
|
| ENSRNOSNP2728091 | ENSRNOT00000006930 | ENSG00000184156 | Epilepsy,_benign_neonatal,_type_2,_121201_(3)
|
| ENSRNOSNP2728091 | ENSRNOT00000030887 | ENSG00000184156 | Epilepsy,_benign_neonatal,_type_2,_121201_(3)
|
| ENSRNOSNP2728180 | ENSRNOT00000018259 | ENSG00000188985 | Anemia,_megaloblastic,_due_to_DHFR_deficiency_(1)_(?)
|
| ENSRNOSNP2728180 | ENSRNOT00000061812 | ENSG00000188985 | Anemia,_megaloblastic,_due_to_DHFR_deficiency_(1)_(?)
|
| ENSRNOSNP2728188 | ENSRNOT00000004686 | ENSG00000036473 | Ornithine_transcarbamylase_deficiency_(3)
|
| ENSRNOSNP2728447 | ENSRNOT00000001766 | ENSG00000186716 | Leukemia,_chronic_myeloid_(3)
|
| ENSRNOSNP2728450 | ENSRNOT00000016167 | ENSG00000141458 | Niemann-Pick_disease,_type_C_(3)
|
| ENSRNOSNP2728450 | ENSRNOT00000016167 | ENSG00000141458 | Niemann-Pick_disease,_type_D,_257250_(2)
|
| ENSRNOSNP2728570 | ENSRNOT00000005237 | ENSG00000091536 | Deafness,_autosomal_recessive_3,_600316_(3)
|
| ENSRNOSNP2728570 | ENSRNOT00000023018 | ENSG00000091536 | Deafness,_autosomal_recessive_3,_600316_(3)
|
| ENSRNOSNP2728570 | ENSRNOT00000045700 | ENSG00000091536 | Deafness,_autosomal_recessive_3,_600316_(3)
|
| ENSRNOSNP2728570 | ENSRNOT00000058047 | ENSG00000091536 | Deafness,_autosomal_recessive_3,_600316_(3)
|
| ENSRNOSNP2728704 | ENSRNOT00000031084 | ENSG00000154646 | Enterokinase_deficiency_(1)
|
| ENSRNOSNP2728704 | ENSRNOT00000031095 | ENSG00000154646 | Enterokinase_deficiency_(1)
|
| ENSRNOSNP2728704 | ENSRNOT00000046665 | ENSG00000154646 | Enterokinase_deficiency_(1)
|
| ENSRNOSNP2728704 | ENSRNOT00000051213 | ENSG00000154646 | Enterokinase_deficiency_(1)
|
| ENSRNOSNP2728829 | ENSRNOT00000022658 | ENSG00000187741 | Fanconi_anemia,_type_A_(3)
|
| ENSRNOSNP2728829 | ENSRNOT00000022658 | ENSG00000187741 | Tyrosinemia,_type_I_(3)
|
| ENSRNOSNP2728855 | ENSRNOT00000023363 | ENSG00000107518 | {Atherosclerosis,_susceptibility_to}_(2)
|
| ENSRNOSNP2728855 | ENSRNOT00000023414 | ENSG00000107518 | {Atherosclerosis,_susceptibility_to}_(2)
|
| ENSRNOSNP2728957 | ENSRNOT00000000744 | ENSG00000150275 | Usher_syndrome,_type_IF_(2)
|
| ENSRNOSNP2729007 | ENSRNOT00000035692 | ENSG00000198947 | Becker_muscular_dystrophy_(3)
|
| ENSRNOSNP2729007 | ENSRNOT00000035692 | ENSG00000198947 | Cardiomyopathy,_dilated,_X-linked_(3)
|
| ENSRNOSNP2729007 | ENSRNOT00000035692 | ENSG00000198947 | Duchenne_muscular_dystrophy_(3)
|
| ENSRNOSNP2729023 | ENSRNOT00000035692 | ENSG00000198947 | Becker_muscular_dystrophy_(3)
|
| ENSRNOSNP2729023 | ENSRNOT00000035692 | ENSG00000198947 | Cardiomyopathy,_dilated,_X-linked_(3)
|
| ENSRNOSNP2729023 | ENSRNOT00000035692 | ENSG00000198947 | Duchenne_muscular_dystrophy_(3)
|
| ENSRNOSNP2729035 | ENSRNOT00000019237 | ENSG00000164344 | Fletcher_factor_deficiency_(1)
|
| ENSRNOSNP2729074 | ENSRNOT00000010796 | ENSG00000059377 | Thromboxane_synthase_deficiency_(2)
|
| ENSRNOSNP2729254 | ENSRNOT00000019174 | ENSG00000156052 | Bleeding_diathesis_due_to_GNAQ_deficiency_(1)
|
| ENSRNOSNP2729398 | ENSRNOT00000028458 | ENSG00000160808 | Cardiomopathy,_hypertrophic,_mid-ventricular_chamber_type_(3)
|
| ENSRNOSNP2729481 | ENSRNOT00000020679 | ENSG00000183873 | Cardiomyopathy,_dilated,_1E_(2)
|
| ENSRNOSNP2729481 | ENSRNOT00000020679 | ENSG00000183873 | Long_QT_syndrome-3_(3)
|
| ENSRNOSNP2729481 | ENSRNOT00000020962 | ENSG00000183873 | Cardiomyopathy,_dilated,_1E_(2)
|
| ENSRNOSNP2729481 | ENSRNOT00000020962 | ENSG00000183873 | Long_QT_syndrome-3_(3)
|
| ENSRNOSNP2729598 | ENSRNOT00000017878 | ENSG00000198691 | Cone-rod_dystrophy_3_(3)
|
| ENSRNOSNP2729598 | ENSRNOT00000017878 | ENSG00000198691 | Fundus_flavimaculatus_with_macular_dystrophy,_248200_(3)
|
| ENSRNOSNP2729598 | ENSRNOT00000017878 | ENSG00000198691 | Retinitis_pigmentosa-19,_601718_(3)
|
| ENSRNOSNP2729598 | ENSRNOT00000017878 | ENSG00000198691 | Retinitis_pigmentosa-19_(2)
|
| ENSRNOSNP2729598 | ENSRNOT00000017878 | ENSG00000198691 | Stargardt_disease-1,_248200_(3)
|
| ENSRNOSNP2729658 | ENSRNOT00000015821 | ENSG00000114125 | Oguchi_disease-1,_258100_(3)
|
| ENSRNOSNP2729986 | ENSRNOT00000016559 | ENSG00000075043 | Epilepsy,_benign,_neonatal,_type_1,_121200_(3)
|
| ENSRNOSNP2729986 | ENSRNOT00000016559 | ENSG00000075043 | Epilepsy,_benign_neonatal,_type_1,_121200_(3)
|
| ENSRNOSNP2729986 | ENSRNOT00000016559 | ENSG00000075043 | Epilepsy,_nocturnal_frontal_lobe,_600513_(3)
|
| ENSRNOSNP2729986 | ENSRNOT00000016574 | ENSG00000075043 | Epilepsy,_benign,_neonatal,_type_1,_121200_(3)
|
| ENSRNOSNP2729986 | ENSRNOT00000016574 | ENSG00000075043 | Epilepsy,_benign_neonatal,_type_1,_121200_(3)
|
| ENSRNOSNP2729986 | ENSRNOT00000016574 | ENSG00000075043 | Epilepsy,_nocturnal_frontal_lobe,_600513_(3)
|
| ENSRNOSNP2729986 | ENSRNOT00000045508 | ENSG00000075043 | Epilepsy,_benign,_neonatal,_type_1,_121200_(3)
|
| ENSRNOSNP2729986 | ENSRNOT00000045508 | ENSG00000075043 | Epilepsy,_benign_neonatal,_type_1,_121200_(3)
|
| ENSRNOSNP2729986 | ENSRNOT00000045508 | ENSG00000075043 | Epilepsy,_nocturnal_frontal_lobe,_600513_(3)
|
| ENSRNOSNP2729986 | ENSRNOT00000049961 | ENSG00000075043 | Epilepsy,_benign,_neonatal,_type_1,_121200_(3)
|
| ENSRNOSNP2729986 | ENSRNOT00000049961 | ENSG00000075043 | Epilepsy,_benign_neonatal,_type_1,_121200_(3)
|
| ENSRNOSNP2729986 | ENSRNOT00000049961 | ENSG00000075043 | Epilepsy,_nocturnal_frontal_lobe,_600513_(3)
|
| ENSRNOSNP2729986 | ENSRNOT00000051170 | ENSG00000075043 | Epilepsy,_benign,_neonatal,_type_1,_121200_(3)
|
| ENSRNOSNP2729986 | ENSRNOT00000051170 | ENSG00000075043 | Epilepsy,_benign_neonatal,_type_1,_121200_(3)
|
| ENSRNOSNP2729986 | ENSRNOT00000051170 | ENSG00000075043 | Epilepsy,_nocturnal_frontal_lobe,_600513_(3)
|
| ENSRNOSNP2729999 | ENSRNOT00000014178 | ENSG00000144891 | Ataxia-telangiectasia_(3)
|
| ENSRNOSNP2729999 | ENSRNOT00000014178 | ENSG00000144891 | B-cell_non-Hodgkin_lymphoma,_sporadic_(3)
|
| ENSRNOSNP2729999 | ENSRNOT00000014178 | ENSG00000144891 | Hypertension,_essential,_145500_(3)
|
| ENSRNOSNP2729999 | ENSRNOT00000014178 | ENSG00000144891 | T-cell_prolymphocytic_leukemia,_sporadic_(3)
|
| ENSRNOSNP2730011 | ENSRNOT00000027367 | ENSG00000124813 | Cleidocranial_dysplasia,_119600_(3)
|
| ENSRNOSNP2730011 | ENSRNOT00000061012 | ENSG00000124813 | Cleidocranial_dysplasia,_119600_(3)
|
| ENSRNOSNP2730011 | ENSRNOT00000061014 | ENSG00000124813 | Cleidocranial_dysplasia,_119600_(3)
|
| ENSRNOSNP2730043 | ENSRNOT00000043612 | ENSG00000113889 | [Kininogen_deficiency]_(3)
|
| ENSRNOSNP2730043 | ENSRNOT00000045361 | ENSG00000113889 | [Kininogen_deficiency]_(3)
|
| ENSRNOSNP2730043 | ENSRNOT00000046666 | ENSG00000113889 | [Kininogen_deficiency]_(3)
|
| ENSRNOSNP2730043 | ENSRNOT00000048338 | ENSG00000113889 | [Kininogen_deficiency]_(3)
|
| ENSRNOSNP2730043 | ENSRNOT00000058478 | ENSG00000113889 | [Kininogen_deficiency]_(3)
|
| ENSRNOSNP2730043 | ENSRNOT00000058479 | ENSG00000113889 | [Kininogen_deficiency]_(3)
|
| ENSRNOSNP2730102 | ENSRNOT00000002343 | ENSG00000198836 | Optic_atrophy_1_(2)
|
| ENSRNOSNP2730118 | ENSRNOT00000007365 | ENSG00000100473 | Deafness,_autosomal_dominant_9_(2)
|
| ENSRNOSNP2730166 | ENSRNOT00000009634 | ENSG00000158125 | Xanthinuria,_type_I_(3)
|
| ENSRNOSNP2730177 | ENSRNOT00000022253 | ENSG00000066468 | Apert_syndrome,_101200_(3)
|
| ENSRNOSNP2730177 | ENSRNOT00000022253 | ENSG00000066468 | Beare-Stevenson_cutis_gyrata_syndrome,_123790_(3)
|
| ENSRNOSNP2730177 | ENSRNOT00000022253 | ENSG00000066468 | Crouzon_craniofacial_dysostosis,_123500_(3)
|
| ENSRNOSNP2730177 | ENSRNOT00000022253 | ENSG00000066468 | Jackson-Weiss_syndrome,_123150_(3)
|
| ENSRNOSNP2730177 | ENSRNOT00000022253 | ENSG00000066468 | Pfeiffer_syndrome,_101600_(3)
|
| ENSRNOSNP2730177 | ENSRNOT00000022289 | ENSG00000066468 | Apert_syndrome,_101200_(3)
|
| ENSRNOSNP2730177 | ENSRNOT00000022289 | ENSG00000066468 | Beare-Stevenson_cutis_gyrata_syndrome,_123790_(3)
|
| ENSRNOSNP2730177 | ENSRNOT00000022289 | ENSG00000066468 | Crouzon_craniofacial_dysostosis,_123500_(3)
|
| ENSRNOSNP2730177 | ENSRNOT00000022289 | ENSG00000066468 | Jackson-Weiss_syndrome,_123150_(3)
|
| ENSRNOSNP2730177 | ENSRNOT00000022289 | ENSG00000066468 | Pfeiffer_syndrome,_101600_(3)
|
| ENSRNOSNP2730177 | ENSRNOT00000022331 | ENSG00000066468 | Apert_syndrome,_101200_(3)
|
| ENSRNOSNP2730177 | ENSRNOT00000022331 | ENSG00000066468 | Beare-Stevenson_cutis_gyrata_syndrome,_123790_(3)
|
| ENSRNOSNP2730177 | ENSRNOT00000022331 | ENSG00000066468 | Crouzon_craniofacial_dysostosis,_123500_(3)
|
| ENSRNOSNP2730177 | ENSRNOT00000022331 | ENSG00000066468 | Jackson-Weiss_syndrome,_123150_(3)
|
| ENSRNOSNP2730177 | ENSRNOT00000022331 | ENSG00000066468 | Pfeiffer_syndrome,_101600_(3)
|
| ENSRNOSNP2730201 | ENSRNOT00000003318 | ENSG00000116690 | Jacobs_syndrome_(2)
|
| ENSRNOSNP2730201 | ENSRNOT00000003250 | ENSG00000116690 | Jacobs_syndrome_(2)
|
| ENSRNOSNP2730201 | ENSRNOT00000059933 | ENSG00000116690 | Jacobs_syndrome_(2)
|
| ENSRNOSNP2730201 | ENSRNOT00000059935 | ENSG00000116690 | Jacobs_syndrome_(2)
|
| ENSRNOSNP2730201 | ENSRNOT00000059937 | ENSG00000116690 | Jacobs_syndrome_(2)
|
| ENSRNOSNP2730268 | ENSRNOT00000002450 | ENSG00000114491 | Oroticaciduria_(3)
|
| ENSRNOSNP2730301 | ENSRNOT00000019237 | ENSG00000164344 | Fletcher_factor_deficiency_(1)
|
| ENSRNOSNP2730496 | ENSRNOT00000050555 | ENSG00000149311 | Ataxia-telangiectasia_(3)
|
| ENSRNOSNP2730496 | ENSRNOT00000050555 | ENSG00000149311 | B-cell_non-Hodgkin_lymphoma,_sporadic_(3)
|
| ENSRNOSNP2730496 | ENSRNOT00000050555 | ENSG00000149311 | T-cell_prolymphocytic_leukemia,_sporadic_(3)
|
| ENSRNOSNP2730544 | ENSRNOT00000019174 | ENSG00000156052 | Bleeding_diathesis_due_to_GNAQ_deficiency_(1)
|
| ENSRNOSNP2730544 | ENSRNOT00000019174 | ENSG00000156052 | Bleeding_diathesis_due_to_GNAQ_deficiency_(1)
|
| ENSRNOSNP2730616 | ENSRNOT00000013103 | ENSG00000184908 | Bartter_syndrome,_type_3_(3)
|
| ENSRNOSNP2730616 | ENSRNOT00000049610 | ENSG00000184908 | Bartter_syndrome,_type_3_(3)
|
| ENSRNOSNP2730661 | ENSRNOT00000017998 | ENSG00000131238 | Ceroid_lipofuscinosis,_neuronal,_variant_juvenile_type,_with_granular_osmiophilic_deposits_(3)
|
| ENSRNOSNP2730661 | ENSRNOT00000017998 | ENSG00000131238 | Ceroid_lipofuscinosis,_neuronal-1,_infantile,_256730_(3)
|
| ENSRNOSNP2730662 | ENSRNOT00000022658 | ENSG00000187741 | Fanconi_anemia,_type_A_(3)
|
| ENSRNOSNP2730662 | ENSRNOT00000022658 | ENSG00000187741 | Tyrosinemia,_type_I_(3)
|
| ENSRNOSNP2730665 | ENSRNOT00000006946 | ENSG00000111670 | Mucolipidosis_III_(1)
|
| ENSRNOSNP2730665 | ENSRNOT00000006946 | ENSG00000111670 | Mucolipidosis_II_(1)
|
| ENSRNOSNP2730665 | ENSRNOT00000006980 | ENSG00000111670 | Mucolipidosis_III_(1)
|
| ENSRNOSNP2730665 | ENSRNOT00000006980 | ENSG00000111670 | Mucolipidosis_II_(1)
|
| ENSRNOSNP2730671 | ENSRNOT00000018202 | ENSG00000109323 | Mannosidosis,_beta-_(3)
|
| ENSRNOSNP2730880 | ENSRNOT00000015750 | ENSG00000053747 | Epidermolysis_bullosa,_junctional,_Herlitz_type_(3)
|
| ENSRNOSNP2730939 | ENSRNOT00000015217 | ENSG00000164258 | Complex_I_deficiency_(3)
|
| ENSRNOSNP2730992 | ENSRNOT00000023363 | ENSG00000107518 | {Atherosclerosis,_susceptibility_to}_(2)
|
| ENSRNOSNP2730992 | ENSRNOT00000023414 | ENSG00000107518 | {Atherosclerosis,_susceptibility_to}_(2)
|
| ENSRNOSNP2731045 | ENSRNOT00000004505 | ENSG00000158813 | Anhidrotic_ectodermal_dysplasia_(2)
|
| ENSRNOSNP2731045 | ENSRNOT00000004505 | ENSG00000158813 | Ectodermal_dysplasia,_hidrotic_(2)
|
| ENSRNOSNP2731200 | ENSRNOT00000013249 | ENSG00000083123 | Maple_syrup_urine_disease,_type_Ib_(3)
|
| ENSRNOSNP2731578 | ENSRNOT00000030168 | ENSG00000102893 | Phosphorylase_kinase_deficiency_of_liver_and_muscle,_261750_(2)_(?)
|
| ENSRNOSNP2731578 | ENSRNOT00000049624 | ENSG00000102893 | Phosphorylase_kinase_deficiency_of_liver_and_muscle,_261750_(2)_(?)
|
| ENSRNOSNP2731630 | ENSRNOT00000016104 | ENSG00000103740 | HPFH,_nondeletion_type_A_(3)
|
| ENSRNOSNP2731644 | ENSRNOT00000045408 | ENSG00000187323 | Colorectal_cancer_(3)
|
| ENSRNOSNP2731737 | ENSRNOT00000000744 | ENSG00000150275 | Usher_syndrome,_type_IF_(2)
|
| ENSRNOSNP2731771 | ENSRNOT00000045408 | ENSG00000187323 | Colorectal_cancer_(3)
|
| ENSRNOSNP2731847 | ENSRNOT00000020466 | ENSG00000075643 | McKusick-Kaufman_syndrome_(2)
|
| ENSRNOSNP2731964 | ENSRNOT00000027925 | ENSG00000110628 | Breast_Cancer_(3)
|
| ENSRNOSNP2731964 | ENSRNOT00000027925 | ENSG00000110628 | Rhabdomyosarcoma,_268210_(3)
|
| ENSRNOSNP2732082 | ENSRNOT00000001738 | ENSG00000174437 | Darier_disease_(keratosis_follicularis)_(2)
|
| ENSRNOSNP2732082 | ENSRNOT00000024347 | ENSG00000174437 | Darier_disease_(keratosis_follicularis)_(2)
|
| ENSRNOSNP2732432 | ENSRNOT00000022658 | ENSG00000187741 | Fanconi_anemia,_type_A_(3)
|
| ENSRNOSNP2732432 | ENSRNOT00000022658 | ENSG00000187741 | Tyrosinemia,_type_I_(3)
|
| ENSRNOSNP2732475 | ENSRNOT00000038652 | ENSG00000081923 | Cholestasis,_benign_recurrent_intrahepatic,_243300_(3)
|
| ENSRNOSNP2732475 | ENSRNOT00000038652 | ENSG00000081923 | Cholestasis,_progressive_familial_intrahepatic-1,_211600_(3)
|
| ENSRNOSNP2732592 | ENSRNOT00000023363 | ENSG00000107518 | {Atherosclerosis,_susceptibility_to}_(2)
|
| ENSRNOSNP2732592 | ENSRNOT00000023414 | ENSG00000107518 | {Atherosclerosis,_susceptibility_to}_(2)
|
| ENSRNOSNP2732838 | ENSRNOT00000035692 | ENSG00000198947 | Becker_muscular_dystrophy_(3)
|
| ENSRNOSNP2732838 | ENSRNOT00000035692 | ENSG00000198947 | Cardiomyopathy,_dilated,_X-linked_(3)
|
| ENSRNOSNP2732838 | ENSRNOT00000035692 | ENSG00000198947 | Duchenne_muscular_dystrophy_(3)
|
| ENSRNOSNP2733048 | ENSRNOT00000006930 | ENSG00000184156 | Epilepsy,_benign_neonatal,_type_2,_121201_(3)
|
| ENSRNOSNP2733048 | ENSRNOT00000030887 | ENSG00000184156 | Epilepsy,_benign_neonatal,_type_2,_121201_(3)
|
| ENSRNOSNP2733258 | ENSRNOT00000045408 | ENSG00000187323 | Colorectal_cancer_(3)
|
| ENSRNOSNP2733419 | ENSRNOT00000045408 | ENSG00000187323 | Colorectal_cancer_(3)
|
| ENSRNOSNP2733520 | ENSRNOT00000005934 | ENSG00000185339 | Transcobalamin_II_deficiency_(3)
|
| ENSRNOSNP2733633 | ENSRNOT00000052292 | ENSG00000188536 | Erythremias,_alpha-_(3)
|
| ENSRNOSNP2733633 | ENSRNOT00000052292 | ENSG00000188536 | Heinz_body_anemias,_alpha-_(3)
|
| ENSRNOSNP2733633 | ENSRNOT00000052292 | ENSG00000188536 | Methemoglobinemias,_alpha-_(3)
|
| ENSRNOSNP2733633 | ENSRNOT00000052292 | ENSG00000188536 | Thalassemias,_alpha-_(3)
|
| ENSRNOSNP2733633 | ENSRNOT00000052292 | ENSG00000206172 | Erythremias,_alpha-_(3)
|
| ENSRNOSNP2733633 | ENSRNOT00000052292 | ENSG00000206172 | Heinz_body_anemias,_alpha-_(3)
|
| ENSRNOSNP2733633 | ENSRNOT00000052292 | ENSG00000206172 | Methemoglobinemias,_alpha-_(3)
|
| ENSRNOSNP2733633 | ENSRNOT00000052292 | ENSG00000206172 | Thalassemias,_alpha-_(3)
|
| ENSRNOSNP2733633 | ENSRNOT00000048977 | ENSG00000188536 | Erythremias,_alpha-_(3)
|
| ENSRNOSNP2733633 | ENSRNOT00000048977 | ENSG00000188536 | Heinz_body_anemias,_alpha-_(3)
|
| ENSRNOSNP2733633 | ENSRNOT00000048977 | ENSG00000188536 | Methemoglobinemias,_alpha-_(3)
|
| ENSRNOSNP2733633 | ENSRNOT00000048977 | ENSG00000188536 | Thalassemias,_alpha-_(3)
|
| ENSRNOSNP2733633 | ENSRNOT00000048977 | ENSG00000206172 | Erythremias,_alpha-_(3)
|
| ENSRNOSNP2733633 | ENSRNOT00000048977 | ENSG00000206172 | Heinz_body_anemias,_alpha-_(3)
|
| ENSRNOSNP2733633 | ENSRNOT00000048977 | ENSG00000206172 | Methemoglobinemias,_alpha-_(3)
|
| ENSRNOSNP2733633 | ENSRNOT00000048977 | ENSG00000206172 | Thalassemias,_alpha-_(3)
|
