Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs12335314
rs12335314 		8 124550784 intron variant T/G snv 1.7E-02
CUI: C1704436
Disease: Peripheral Arterial Diseases
Peripheral Arterial Diseases 		Cardiovascular Diseases 0.700 1.000 1 2016 2016
dbSNP: rs776388520
rs776388520 		1.000 8 124543176 missense variant T/C snv 1.6E-05 1.4E-05
CUI: C4748803
Disease: MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 24
MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 24 		0.700 1.000 1 2012 2012