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: rs2681492
rs2681492
ATP2B1
0.925 0.040 12 89619312 intron variant T/C;G snv
CUI: C0005823
Disease: Blood Pressure
Blood Pressure 		0.700 1.000 2 2011 2013
dbSNP: rs2681492
rs2681492
ATP2B1
0.925 0.040 12 89619312 intron variant T/C;G snv
CUI: C1306620
Disease: Systolic blood pressure measurement
Systolic blood pressure measurement 		0.700 1.000 1 2009 2009
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