Hepatoencephalopathy Due to Combined Oxidative Phosphorylation Defect Type 1

Other 143 variants 1 gene

Upload your DNA to see your personal risk score for Hepatoencephalopathy Due to Combined Oxidative Phosphorylation Defect Type 1.

Associated Genes (1)
Associated Variants (143)
RSID Gene Risk Allele Odds Ratio Evidence
RS1314096195 GFM1 strong
RS2473036507 GFM1 strong
RS866873846 GFM1 strong
RS1722355988 GFM1 strong
RS756718556 GFM1 strong
RS1281034886 GFM1 strong
RS2473938268 GFM1 strong
RS2473046112 GFM1 strong
RS2108051038 GFM1 strong
RS2473938802 GFM1 strong
RS2473971829 GFM1 strong
RS2473960497 GFM1 strong
RS2473993041 GFM1 strong
RS1416173655 GFM1 strong
RS2473949734 GFM1 strong
RS2473045397 GFM1 strong
RS2473938700 GFM1 strong
RS2473949135 GFM1 strong
RS2473064367 GFM1 strong
RS1434843098 GFM1 strong
RS2474011501 GFM1 strong
RS1721792587 GFM1 strong
RS955729561 GFM1 strong
RS768006278 GFM1 strong
RS1437640913 GFM1 strong
RS771890880 GFM1 strong
RS779253646 GFM1 strong
RS2108016910 GFM1 strong
RS147620098 GFM1 strong
RS1560135485 GFM1 strong
RS1725442904 GFM1 strong
RS763344414 GFM1 strong
RS775228051 GFM1 strong
RS1721717504 GFM1 strong
RS1449057162 GFM1 strong
RS768112611 GFM1 strong
RS778902849 GFM1 strong
RS1263604546 GFM1 strong
RS774976760 GFM1 strong
RS889180452 GFM1 strong
RS1225913995 GFM1 strong
RS760266828 GFM1 strong
RS1721865059 GFM1 strong
RS2108102423 GFM1 strong
RS763423294 GFM1 strong
RS1214047183 GFM1 strong
RS1332636394 GFM1 strong
RS1456835520 GFM1 strong
RS750287727 GFM1 strong
RS760290078 GFM1 strong
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