Source: GWASDB

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: rs4773144
rs4773144
0.827 0.080 13 110308365 intron variant A/G snv 0.42
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.810 1.000 2 2011 2016
dbSNP: rs4773144
rs4773144
0.827 0.080 13 110308365 intron variant A/G snv 0.42
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.700 1.000 1 2013 2013
dbSNP: rs4773144
rs4773144
0.827 0.080 13 110308365 intron variant A/G snv 0.42
CORONARY ARTERY DISEASE, AUTOSOMAL DOMINANT, 1
0.700 1.000 1 2013 2013