Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs2505083
rs2505083
JCAD
0.882 0.080 10 30046193 intron variant T/C snv 0.33
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		0.800 1.000 1 2011 2011
dbSNP: rs2505083
rs2505083
JCAD
0.882 0.080 10 30046193 intron variant T/C snv 0.33
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		0.700 1.000 1 2015 2015