Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs587776944
rs587776944
Entrez Id: 58495;92667
Gene Symbol: OVOL2;MGME1
OVOL2;MGME1
CUI: C3554462
Disease:
MITOCHONDRIAL DNA DEPLETION SYNDROME 11
G 0.700 CausalMutation CLINVAR