rs2681472, ATP2B1

N. diseases: 9
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 0.882 0.080 12 89615182 intron variant A/G snv 0.14 0.860 1.000 8 2009 2019
Blood Pressure
CUI: C0005823
Disease: Blood Pressure
220 0.882 0.080 12 89615182 intron variant A/G snv 0.14 0.700 1.000 2 2011 2011
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.882 0.080 12 89615182 intron variant A/G snv 0.14 0.700 1.000 2 2015 2017
Diastolic blood pressure
CUI: C0428883
Disease: Diastolic blood pressure
1037 0.882 0.080 12 89615182 intron variant A/G snv 0.14 0.700 1.000 2 2009 2018
Mean blood pressure
CUI: C0428886
Disease: Mean blood pressure
344 0.882 0.080 12 89615182 intron variant A/G snv 0.14 0.700 1.000 2 2016 2018
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.882 0.080 12 89615182 intron variant A/G snv 0.14 0.700 1.000 1 2011 2011
Diastolic blood pressure measurement
81 0.882 0.080 12 89615182 intron variant A/G snv 0.14 0.700 1.000 1 2009 2009
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
680 0.882 0.080 12 89615182 intron variant A/G snv 0.14 0.700 1.000 1 2015 2015
Systolic Pressure
CUI: C0871470
Disease: Systolic Pressure
1931 0.882 0.080 12 89615182 intron variant A/G snv 0.14 0.700 1.000 1 2018 2018