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: 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 3 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
CUI: C0032181
Disease: Platelet Count measurement
Platelet Count measurement
0.800 1.000 3 2011 2016
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 2 2009 2019
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 2 2012 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 2 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: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.800 1.000 1 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
Low density lipoprotein cholesterol measurement
0.800 1.000 1 2012 2018
dbSNP: rs3184504
rs3184504
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.730 1.000 4 2015 2019
dbSNP: rs3184504
rs3184504
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases
0.720 1.000 1 2019 2019
dbSNP: rs3184504
rs3184504
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67
CUI: C0241910
Disease: Autoimmune Chronic Hepatitis
Autoimmune Chronic Hepatitis
0.720 1.000 1 2014 2017
dbSNP: rs3184504
rs3184504
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung
0.710 1.000 1 2015 2016
dbSNP: rs3184504
rs3184504
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
0.710 1.000 1 2015 2016
dbSNP: rs3184504
rs3184504
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67
CUI: C0476089
Disease: Endometrial Carcinoma
Endometrial Carcinoma
0.710 1.000 1 2015 2018
dbSNP: rs3184504
rs3184504
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure
0.700 1.000 10 2009 2019
dbSNP: rs3184504
rs3184504
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure
0.700 1.000 5 2009 2018
dbSNP: rs3184504
rs3184504
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67
CUI: C0007102
Disease: Malignant tumor of colon
Malignant tumor of colon
0.700 1.000 4 2015 2019
dbSNP: rs3184504
rs3184504
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67
COLORECTAL CANCER, SUSCEPTIBILITY TO, 3
0.700 1.000 4 2015 2019
dbSNP: rs3184504
rs3184504
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67
COLORECTAL CANCER, SUSCEPTIBILITY TO, 12
0.700 1.000 4 2015 2019
dbSNP: rs3184504
rs3184504
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
0.700 1.000 4 2015 2019
dbSNP: rs3184504
rs3184504
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67
CUI: C0009404
Disease: Colorectal Neoplasms
Colorectal Neoplasms
0.700 1.000 4 2015 2019