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
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
dbSNP: rs3184504
rs3184504
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67
CUI: C1319315
Disease: Adenocarcinoma of large intestine
Adenocarcinoma of large intestine
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
Malignant neoplasm of large intestine
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: 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
COLORECTAL CANCER, SUSCEPTIBILITY TO, 1
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: 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: C0008313
Disease: Cholangitis, Sclerosing
Cholangitis, Sclerosing
0.700 1.000 3 2013 2017
dbSNP: rs3184504
rs3184504
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67
CUI: C0518015
Disease: Hemoglobin measurement
Hemoglobin measurement
0.700 1.000 3 2012 2017
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: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure
0.700 1.000 2 2016 2019
dbSNP: rs3184504
rs3184504
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 2 2018 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: 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: rs739496
rs739496
0.790 0.160 12 111449855 3 prime UTR variant A/G snv 0.27
CUI: C0032181
Disease: Platelet Count measurement
Platelet Count measurement
0.700 1.000 2 2010 2014
dbSNP: rs11065904
rs11065904
0.882 0.080 12 111449163 3 prime UTR variant T/A snv 3.2E-02
CUI: C0005845
Disease: Blood urea nitrogen measurement
Blood urea nitrogen measurement
0.700 1.000 1 2019 2019
dbSNP: rs148636776
rs148636776
0.790 0.280 12 111447491 missense variant G/A snv 1.5E-04 2.4E-04
CUI: C0032181
Disease: Platelet Count measurement
Platelet Count measurement
0.700 1.000 1 2016 2016
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