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: rs79105258
rs79105258
12 111280427 intron variant C/A;T snv
CUI: C0202239
Disease: Uric acid measurement (procedure)
Uric acid measurement (procedure)
0.700 1.000 3 2018 2019
dbSNP: rs79105258
rs79105258
12 111280427 intron variant C/A;T snv
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure
0.700 1.000 2 2018 2018
dbSNP: rs79105258
rs79105258
12 111280427 intron variant C/A;T snv
CUI: C0017654
Disease: Glomerular Filtration Rate
Glomerular Filtration Rate
0.700 1.000 2 2018 2019
dbSNP: rs79105258
rs79105258
12 111280427 intron variant C/A;T snv
CUI: C0428886
Disease: Mean blood pressure
Mean blood pressure
0.700 1.000 2 2018 2018
dbSNP: rs79105258
rs79105258
12 111280427 intron variant C/A;T snv
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure
0.700 1.000 2 2018 2018
dbSNP: rs79105258
rs79105258
12 111280427 intron variant C/A;T snv
Aspartate aminotransferase measurement
0.700 1.000 1 2018 2018
dbSNP: rs79105258
rs79105258
12 111280427 intron variant C/A;T snv
Serum gamma-glutamyl transferase measurement
0.700 1.000 1 2018 2018
dbSNP: rs79105258
rs79105258
12 111280427 intron variant C/A;T snv
Alanine aminotransferase measurement
0.700 1.000 1 2018 2018
dbSNP: rs79105258
rs79105258
12 111280427 intron variant C/A;T snv
CUI: C0005845
Disease: Blood urea nitrogen measurement
Blood urea nitrogen measurement
0.700 1.000 1 2018 2018
dbSNP: rs79105258
rs79105258
12 111280427 intron variant C/A;T snv
CUI: C0337438
Disease: Glucose measurement
Glucose measurement
0.700 1.000 1 2018 2018
dbSNP: rs79105258
rs79105258
12 111280427 intron variant C/A;T snv
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result)
0.700 1.000 1 2018 2018
dbSNP: rs79105258
rs79105258
12 111280427 intron variant C/A;T snv
CUI: C0337443
Disease: Sodium measurement
Sodium measurement
0.700 1.000 1 2018 2018
dbSNP: rs79105258
rs79105258
12 111280427 intron variant C/A;T snv
Finding of Mean Corpuscular Hemoglobin
0.700 1.000 1 2018 2018
dbSNP: rs79105258
rs79105258
12 111280427 intron variant C/A;T snv
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement
0.700 1.000 1 2018 2018
dbSNP: rs79105258
rs79105258
12 111280427 intron variant C/A;T snv
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.700 1.000 1 2018 2018
dbSNP: rs79105258
rs79105258
12 111280427 intron variant C/A;T snv
Serum Alanine Aminotransferase Measurement
0.700 1.000 1 2018 2018
dbSNP: rs79105258
rs79105258
12 111280427 intron variant C/A;T snv
High density lipoprotein measurement
0.700 1.000 1 2018 2018
dbSNP: rs79105258
rs79105258
12 111280427 intron variant C/A;T snv
Creatinine measurement, serum (procedure)
0.700 1.000 1 2018 2018
dbSNP: rs79105258
rs79105258
12 111280427 intron variant C/A;T snv
Activated Partial Thromboplastin Time measurement
0.700 1.000 1 2018 2018
dbSNP: rs79105258
rs79105258
12 111280427 intron variant C/A;T snv
CUI: C0201952
Disease: Chloride measurement
Chloride measurement
0.700 1.000 1 2018 2018
dbSNP: rs79105258
rs79105258
12 111280427 intron variant C/A;T snv
CUI: C0495706
Disease: elevated blood glucose level
elevated blood glucose level
0.700 1.000 1 2018 2018
dbSNP: rs79105258
rs79105258
12 111280427 intron variant C/A;T snv
Low density lipoprotein cholesterol measurement
0.700 1.000 1 2018 2018
dbSNP: rs79105258
rs79105258
12 111280427 intron variant C/A;T snv
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2018 2018