Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs137973334
rs137973334
G 0.800 CausalMutation CLINVAR

dbSNP: rs767568897
rs767568897
T 0.800 CausalMutation CLINVAR

dbSNP: rs786205156
rs786205156
G 0.800 CausalMutation CLINVAR

dbSNP: rs137891647
rs137891647
G 0.700 CausalMutation CLINVAR Mutations in human lipoyltransferase gene LIPT1 cause a Leigh disease with secondary deficiency for pyruvate and alpha-ketoglutarate dehydrogenase. 24341803

2013