rs12579302, ATP2B1

N. diseases: 19
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.
Systolic Pressure
CUI: C0871470
Disease: Systolic Pressure
1931 0.851 0.120 12 89656726 intron variant A/G snv 0.15 0.700 1.000 5 2016 2019
Diastolic blood pressure
CUI: C0428883
Disease: Diastolic blood pressure
1037 0.851 0.120 12 89656726 intron variant A/G snv 0.15 0.700 1.000 2 2016 2018
Mean blood pressure
CUI: C0428886
Disease: Mean blood pressure
344 0.851 0.120 12 89656726 intron variant A/G snv 0.15 0.700 1.000 2 2017 2018
Alcohol consumption
CUI: C0001948
Disease: Alcohol consumption
535 0.851 0.120 12 89656726 intron variant A/G snv 0.15 0.700 1.000 1 2018 2018
Atrial Fibrillation
CUI: C0004238
Disease: Atrial Fibrillation
584 0.851 0.120 12 89656726 intron variant A/G snv 0.15 0.700 1.000 1 2016 2016
Body mass index
CUI: C1305855
Disease: Body mass index
2689 0.851 0.120 12 89656726 intron variant A/G snv 0.15 0.700 1.000 1 2016 2016
Cerebrovascular accident
CUI: C0038454
Disease: Cerebrovascular accident
591 0.851 0.120 12 89656726 intron variant A/G snv 0.15 0.700 1.000 1 2016 2016
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.851 0.120 12 89656726 intron variant A/G snv 0.15 0.700 1.000 1 2016 2016
Diabetes
CUI: C0011847
Disease: Diabetes
710 0.851 0.120 12 89656726 intron variant A/G snv 0.15 0.700 1.000 1 2016 2016
Diabetes Mellitus
CUI: C0011849
Disease: Diabetes Mellitus
824 0.851 0.120 12 89656726 intron variant A/G snv 0.15 0.700 1.000 1 2016 2016
elevated blood glucose level
CUI: C0495706
Disease: elevated blood glucose level
111 0.851 0.120 12 89656726 intron variant A/G snv 0.15 0.700 1.000 1 2016 2016
Glucose measurement
CUI: C0337438
Disease: Glucose measurement
111 0.851 0.120 12 89656726 intron variant A/G snv 0.15 0.700 1.000 1 2016 2016
Heart failure
CUI: C0018801
Disease: Heart failure
201 0.851 0.120 12 89656726 intron variant A/G snv 0.15 0.700 1.000 1 2016 2016
Hematocrit procedure
CUI: C0018935
Disease: Hematocrit procedure
216 0.851 0.120 12 89656726 intron variant A/G snv 0.15 0.700 1.000 1 2016 2016
High density lipoprotein measurement
1440 0.851 0.120 12 89656726 intron variant A/G snv 0.15 0.700 1.000 1 2016 2016
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 0.851 0.120 12 89656726 intron variant A/G snv 0.15 0.700 1.000 1 2018 2018
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.851 0.120 12 89656726 intron variant A/G snv 0.15 0.700 1.000 1 2016 2016
Serum total cholesterol measurement
CUI: C1445957
Disease: Serum total cholesterol measurement
1243 0.851 0.120 12 89656726 intron variant A/G snv 0.15 0.700 1.000 1 2016 2016
Triglycerides measurement
CUI: C0202236
Disease: Triglycerides measurement
1418 0.851 0.120 12 89656726 intron variant A/G snv 0.15 0.700 1.000 1 2016 2016