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: rs12579302
rs12579302
0.851 0.120 12 89656726 intron variant A/G snv 0.15
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure
0.700 1.000 5 2016 2019
dbSNP: rs12579302
rs12579302
0.851 0.120 12 89656726 intron variant A/G snv 0.15
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure
0.700 1.000 2 2016 2018
dbSNP: rs12579302
rs12579302
0.851 0.120 12 89656726 intron variant A/G snv 0.15
CUI: C0428886
Disease: Mean blood pressure
Mean blood pressure
0.700 1.000 2 2017 2018
dbSNP: rs12579302
rs12579302
0.851 0.120 12 89656726 intron variant A/G snv 0.15
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.700 1.000 1 2016 2016
dbSNP: rs12579302
rs12579302
0.851 0.120 12 89656726 intron variant A/G snv 0.15
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.700 1.000 1 2016 2016
dbSNP: rs12579302
rs12579302
0.851 0.120 12 89656726 intron variant A/G snv 0.15
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation
0.700 1.000 1 2016 2016
dbSNP: rs12579302
rs12579302
0.851 0.120 12 89656726 intron variant A/G snv 0.15
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2016 2016
dbSNP: rs12579302
rs12579302
0.851 0.120 12 89656726 intron variant A/G snv 0.15
CUI: C0038454
Disease: Cerebrovascular accident
Cerebrovascular accident
0.700 1.000 1 2016 2016
dbSNP: rs12579302
rs12579302
0.851 0.120 12 89656726 intron variant A/G snv 0.15
CUI: C0495706
Disease: elevated blood glucose level
elevated blood glucose level
0.700 1.000 1 2016 2016
dbSNP: rs12579302
rs12579302
0.851 0.120 12 89656726 intron variant A/G snv 0.15
CUI: C0001948
Disease: Alcohol consumption
Alcohol consumption
0.700 1.000 1 2018 2018
dbSNP: rs12579302
rs12579302
0.851 0.120 12 89656726 intron variant A/G snv 0.15
High density lipoprotein measurement
0.700 1.000 1 2016 2016
dbSNP: rs12579302
rs12579302
0.851 0.120 12 89656726 intron variant A/G snv 0.15
CUI: C0011847
Disease: Diabetes
Diabetes
0.700 1.000 1 2016 2016
dbSNP: rs12579302
rs12579302
0.851 0.120 12 89656726 intron variant A/G snv 0.15
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.700 1.000 1 2018 2018
dbSNP: rs12579302
rs12579302
0.851 0.120 12 89656726 intron variant A/G snv 0.15
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.700 1.000 1 2016 2016
dbSNP: rs12579302
rs12579302
0.851 0.120 12 89656726 intron variant A/G snv 0.15
CUI: C0018935
Disease: Hematocrit procedure
Hematocrit procedure
0.700 1.000 1 2016 2016
dbSNP: rs12579302
rs12579302
0.851 0.120 12 89656726 intron variant A/G snv 0.15
CUI: C0018801
Disease: Heart failure
Heart failure
0.700 1.000 1 2016 2016
dbSNP: rs12579302
rs12579302
0.851 0.120 12 89656726 intron variant A/G snv 0.15
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 1 2016 2016
dbSNP: rs12579302
rs12579302
0.851 0.120 12 89656726 intron variant A/G snv 0.15
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus
0.700 1.000 1 2016 2016
dbSNP: rs12579302
rs12579302
0.851 0.120 12 89656726 intron variant A/G snv 0.15
CUI: C0337438
Disease: Glucose measurement
Glucose measurement
0.700 1.000 1 2016 2016