Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs199476132
rs199476132
Entrez Id: 4512;4513;4536;4570
Gene Symbol: COX1;COX2;ND2;TRNN
COX1;COX2;ND2;TRNN
CUI: C0268237
Disease:
Cytochrome-c Oxidase Deficiency
C 0.700 CausalMutation CLINVAR