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: rs7136259
rs7136259
ATP2B1
1.000 0.040 12 89687411 intron variant T/A;C;G snv
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		0.800 1.000 1 2012 2012
dbSNP: rs2681472
rs2681472
ATP2B1
0.882 0.080 12 89615182 intron variant A/G snv 0.14
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		0.700 1.000 1 2011 2011
dbSNP: rs2681492
rs2681492
ATP2B1
0.925 0.040 12 89619312 intron variant T/C;G snv
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		0.700 1.000 1 2011 2011