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
0.642 0.393 12 111446804 missense variant T/A,C,G snp 0.67 0.67
Diabetes Mellitus, Insulin-Dependent
0.810 1.000 2 2010 2012
dbSNP: rs3184504
rs3184504
0.642 0.393 12 111446804 missense variant T/A,C,G snp 0.67 0.67
CUI: C0032181
Disease: Platelet Count measurement
Platelet Count measurement
0.800 3 2011 2017
dbSNP: rs3184504
rs3184504
0.642 0.393 12 111446804 missense variant T/A,C,G snp 0.67 0.67
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.800 2 2009 2017
dbSNP: rs3184504
rs3184504
0.642 0.393 12 111446804 missense variant T/A,C,G snp 0.67 0.67
CUI: C0750879
Disease: Eosinophil count result
Eosinophil count result
0.800 2 2009 2017
dbSNP: rs3184504
rs3184504
0.642 0.393 12 111446804 missense variant T/A,C,G snp 0.67 0.67
CUI: C0008313
Disease: Cholangitis, Sclerosing
Cholangitis, Sclerosing
0.800 2 2013 2017
dbSNP: rs3184504
rs3184504
0.642 0.393 12 111446804 missense variant T/A,C,G snp 0.67 0.67
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.800 2 2013 2018
dbSNP: rs3184504
rs3184504
0.642 0.393 12 111446804 missense variant T/A,C,G snp 0.67 0.67
CUI: C0007570
Disease: Celiac Disease
Celiac Disease
0.800 1 2012 2012
dbSNP: rs3184504
rs3184504
0.642 0.393 12 111446804 missense variant T/A,C,G snp 0.67 0.67
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.800 1 2011 2014
dbSNP: rs3184504
rs3184504
0.642 0.393 12 111446804 missense variant T/A,C,G snp 0.67 0.67
CUI: C0020676
Disease: Hypothyroidism
Hypothyroidism
0.800 1 2012 2012
dbSNP: rs3184504
rs3184504
0.642 0.393 12 111446804 missense variant T/A,C,G snp 0.67 0.67
CUI: C0201910
Disease: Beta-2-microglobulin measurement
Beta-2-microglobulin measurement
0.800 1 2013 2013
dbSNP: rs3184504
rs3184504
0.642 0.393 12 111446804 missense variant T/A,C,G snp 0.67 0.67
CUI: C1527249
Disease: Colorectal Cancer
Colorectal Cancer
0.730 1.000 2 2015 2016
dbSNP: rs3184504
rs3184504
0.642 0.393 12 111446804 missense variant T/A,C,G snp 0.67 0.67
CUI: C0241910
Disease: Hepatitis, Autoimmune
Hepatitis, Autoimmune
0.710 1.000 1 2014 2014
dbSNP: rs3184504
rs3184504
0.642 0.393 12 111446804 missense variant T/A,C,G snp 0.67 0.67
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure
0.700 4 2010 2017
dbSNP: rs3184504
rs3184504
0.642 0.393 12 111446804 missense variant T/A,C,G snp 0.67 0.67
CUI: C0518015
Disease: Hemoglobin measurement
Hemoglobin measurement
0.700 3 2012 2017
dbSNP: rs3184504
rs3184504
0.642 0.393 12 111446804 missense variant T/A,C,G snp 0.67 0.67
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure
0.700 2 2010 2017
dbSNP: rs739496
rs739496
1.000 0.071 12 111449855 3 prime UTR variant A/G snp 0.28
CUI: C0032181
Disease: Platelet Count measurement
Platelet Count measurement
0.700 2 2010 2014
dbSNP: rs11065898
rs11065898
1.000 0.036 12 111424771 intron variant C/T snp 0.21
CUI: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis
0.700 1 2013 2013
dbSNP: rs148636776
rs148636776
12 111447491 missense variant G/A snp 1.5E-04 1.6E-04
CUI: C0474566
Disease: Platelet hematocrit measurement
Platelet hematocrit measurement
0.700 1 2017 2017
dbSNP: rs148636776
rs148636776
12 111447491 missense variant G/A snp 1.5E-04 1.6E-04
CUI: C0032181
Disease: Platelet Count measurement
Platelet Count measurement
0.700 1 2017 2017
dbSNP: rs3184504
rs3184504
0.642 0.393 12 111446804 missense variant T/A,C,G snp 0.67 0.67
CUI: C0857490
Disease: Granulocyte count
Granulocyte count
0.700 1 2017 2017
dbSNP: rs3184504
rs3184504
0.642 0.393 12 111446804 missense variant T/A,C,G snp 0.67 0.67
CUI: C0033860
Disease: Psoriasis
Psoriasis
0.700 1 2017 2017
dbSNP: rs3184504
rs3184504
0.642 0.393 12 111446804 missense variant T/A,C,G snp 0.67 0.67
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases
0.700 1 2016 2016
dbSNP: rs3184504
rs3184504
0.642 0.393 12 111446804 missense variant T/A,C,G snp 0.67 0.67
CUI: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis
0.700 1 2017 2017
dbSNP: rs3184504
rs3184504
0.642 0.393 12 111446804 missense variant T/A,C,G snp 0.67 0.67
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure
0.700 1 2017 2017
dbSNP: rs3184504
rs3184504
0.642 0.393 12 111446804 missense variant T/A,C,G snp 0.67 0.67
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.700 1 2017 2017