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: rs2681472
rs2681472
ATP2B1
0.882 0.080 12 89615182 intron variant A/G snv 0.14
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.700 1.000 2 2015 2017
dbSNP: rs2681492
rs2681492
ATP2B1
0.925 0.040 12 89619312 intron variant T/C;G snv
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.700 1.000 1 2018 2018
dbSNP: rs57481061
rs57481061
ATP2B1
1.000 0.040 12 89625401 intron variant C/G snv 0.14
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.700 1.000 1 2018 2018