Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121434427
rs121434427
MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 6
0.800 GeneticVariation UNIPROT Mutations in the complex I NDUFS2 gene of patients with cardiomyopathy and encephalomyopathy. 11220739

2001