Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121434462
rs121434462
Entrez Id: 4538;4540;4568
Gene Symbol: ND4;ND5;TRNL2
ND4;ND5;TRNL2
CUI: C0162666
Disease:
Mitochondrial Encephalomyopathies
A 0.700 CausalMutation CLINVAR