Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs398124308
rs398124308
GGAGT 0.700 GeneticVariation CLINVAR Mutation screening of 75 candidate genes in 152 complex I deficiency cases identifies pathogenic variants in 16 genes including NDUFB9. 22200994

2012

dbSNP: rs373075574
rs373075574
T 0.700 CausalMutation CLINVAR

dbSNP: rs536400690
rs536400690
C 0.700 GeneticVariation CLINVAR