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: rs2681472
rs2681472
ATP2B1
0.882 0.080 12 89615182 intron variant A/G snv 0.14
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		0.860 1.000 1 2009 2019
dbSNP: rs2681472
rs2681472
ATP2B1
0.882 0.080 12 89615182 intron variant A/G snv 0.14
CUI: C0005823
Disease: Blood Pressure
Blood Pressure 		0.700 1.000 2 2011 2011
dbSNP: rs2681472
rs2681472
ATP2B1
0.882 0.080 12 89615182 intron variant A/G snv 0.14
CUI: C1305849
Disease: Diastolic blood pressure measurement
Diastolic blood pressure measurement 		0.700 1.000 1 2009 2009
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