Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs587776438
rs587776438
COX3 ; ND3 ; ND4 ; ND4L
A 0.700 CausalMutation CLINVAR Leigh disease presenting in utero due to a novel missense mutation in the mitochondrial DNA-ND3. 20202874

2010