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: rs2681492
rs2681492
ATP2B1
0.925 0.040 12 89619312 intron variant T/C;G snv
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		0.710 1.000 1 2013 2018
dbSNP: rs2681492
rs2681492
ATP2B1
0.925 0.040 12 89619312 intron variant T/C;G snv
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 3 2009 2018
dbSNP: rs2681492
rs2681492
ATP2B1
0.925 0.040 12 89619312 intron variant T/C;G snv
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure 		0.700 1.000 2 2017 2018
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: rs2681492
rs2681492
ATP2B1
0.925 0.040 12 89619312 intron variant T/C;G snv
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases 		0.700 1.000 1 2019 2019
dbSNP: rs2681492
rs2681492
ATP2B1
0.925 0.040 12 89619312 intron variant T/C;G snv
CUI: C0428886
Disease: Mean blood pressure
Mean blood pressure 		0.700 1.000 1 2018 2018
dbSNP: rs2681492
rs2681492
ATP2B1
0.925 0.040 12 89619312 intron variant T/C;G snv
CUI: C0001948
Disease: Alcohol consumption
Alcohol consumption 		0.700 1.000 1 2018 2018