Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs12335314
rs12335314
Entrez Id: 4715;9788
Gene Symbol: NDUFB9;MTSS1
NDUFB9;MTSS1
CUI: C1704436
Disease:
Peripheral Arterial Diseases 		0.700 GeneticVariation GWASCAT Genetic Variants in the Bone Morphogenic Protein Gene Family Modify the Association between Residential Exposure to Traffic and Peripheral Arterial Disease. 27082954 2016
dbSNP: rs776388520
rs776388520
Entrez Id: 4715
Gene Symbol: NDUFB9
NDUFB9
CUI: C4748803
Disease:
MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 24 		0.700 GeneticVariation UNIPROT Mutation screening of 75 candidate genes in 152 complex I deficiency cases identifies pathogenic variants in 16 genes including NDUFB9. 22200994 2012