Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs28384199
rs28384199
ND4 ; ND5
A 0.700 CausalMutation CLINVAR Clinical and molecular findings in children with complex I deficiency. 15576045

2004
dbSNP: rs28384199
rs28384199
ND4 ; ND5
A 0.700 CausalMutation CLINVAR A novel mtDNA C11777A mutation in Leigh syndrome. 16120329

2003