Source: GWASDB

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: rs3184504
rs3184504
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67
Diabetes Mellitus, Insulin-Dependent
0.820 1.000 2 2009 2018
dbSNP: rs3184504
rs3184504
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.820 1.000 1 2011 2018
dbSNP: rs3184504
rs3184504
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.810 1.000 2 2013 2018
dbSNP: rs3184504
rs3184504
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67
CUI: C0007570
Disease: Celiac Disease
Celiac Disease
0.810 1.000 1 2011 2015
dbSNP: rs3184504
rs3184504
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67
Low density lipoprotein cholesterol measurement
0.800 1.000 2 2012 2018
dbSNP: rs3184504
rs3184504
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67
CUI: C0032181
Disease: Platelet Count measurement
Platelet Count measurement
0.800 1.000 2 2011 2016
dbSNP: rs3184504
rs3184504
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.800 1.000 2 2012 2018
dbSNP: rs3184504
rs3184504
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67
CUI: C0201910
Disease: Beta-2-microglobulin measurement
Beta-2-microglobulin measurement
0.800 1.000 1 2013 2013
dbSNP: rs3184504
rs3184504
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement
0.800 1.000 1 2009 2019
dbSNP: rs3184504
rs3184504
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.800 1.000 1 2009 2016
dbSNP: rs3184504
rs3184504
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67
CUI: C1272321
Disease: Autoantibody measurement
Autoantibody measurement
0.800 1.000 1 2011 2018
dbSNP: rs3184504
rs3184504
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67
CUI: C0020676
Disease: Hypothyroidism
Hypothyroidism
0.800 1.000 1 2012 2019
dbSNP: rs3184504
rs3184504
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67
Diastolic blood pressure measurement
0.700 1.000 3 2009 2013
dbSNP: rs3184504
rs3184504
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement
0.700 1.000 2 2012 2013
dbSNP: rs3184504
rs3184504
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67
CUI: C1306620
Disease: Systolic blood pressure measurement
Systolic blood pressure measurement
0.700 1.000 2 2009 2013
dbSNP: rs3184504
rs3184504
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67
CUI: C0566602
Disease: Primary sclerosing cholangitis
Primary sclerosing cholangitis
0.700 1.000 1 2013 2013
dbSNP: rs3184504
rs3184504
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs3184504
rs3184504
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67
CUI: C0004364
Disease: Autoimmune Diseases
Autoimmune Diseases
0.700 1.000 1 2011 2011
dbSNP: rs3184504
rs3184504
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67
CUI: C0003868
Disease: Arthritis, Gouty
Arthritis, Gouty
0.700 1.000 1 2013 2013
dbSNP: rs3184504
rs3184504
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis
0.700 1.000 1 2012 2012
dbSNP: rs3184504
rs3184504
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67
CUI: C0018099
Disease: Gout
Gout
0.700 1.000 1 2013 2013
dbSNP: rs3184504
rs3184504
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67
CUI: C0021053
Disease: Immune System Diseases
Immune System Diseases
0.700 1.000 1 2011 2011
dbSNP: rs3184504
rs3184504
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67
CUI: C0005823
Disease: Blood Pressure
Blood Pressure
0.700 1.000 1 2011 2011
dbSNP: rs3184504
rs3184504
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67
CUI: C0039685
Disease: Tetralogy of Fallot
Tetralogy of Fallot
0.700 1.000 1 2013 2013