Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121434468
rs121434468
COX1 ; ND1 ; ND2 ; TRNI
A 0.700 GeneticVariation CLINVAR Novel heteroplasmic mtDNA mutation in a family with heterogeneous clinical presentations. 11782991

2002