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: rs4246215
rs4246215
0.677 0.320 11 61796827 3 prime UTR variant G/C;T snv
CUI: C0007102
Disease: Malignant tumor of colon
Malignant tumor of colon
0.700 1.000 1 2019 2019
dbSNP: rs4246215
rs4246215
0.677 0.320 11 61796827 3 prime UTR variant G/C;T snv
COLORECTAL CANCER, SUSCEPTIBILITY TO, 3
0.700 1.000 1 2019 2019
dbSNP: rs4246215
rs4246215
0.677 0.320 11 61796827 3 prime UTR variant G/C;T snv
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.800 1.000 1 2014 2019
dbSNP: rs4246215
rs4246215
0.677 0.320 11 61796827 3 prime UTR variant G/C;T snv
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases
0.800 1.000 1 2012 2012
dbSNP: rs4246215
rs4246215
0.677 0.320 11 61796827 3 prime UTR variant G/C;T snv
COLORECTAL CANCER, SUSCEPTIBILITY TO, 1
0.700 1.000 1 2019 2019
dbSNP: rs4246215
rs4246215
0.677 0.320 11 61796827 3 prime UTR variant G/C;T snv
CUI: C1319315
Disease: Adenocarcinoma of large intestine
Adenocarcinoma of large intestine
0.700 1.000 1 2019 2019
dbSNP: rs4246215
rs4246215
0.677 0.320 11 61796827 3 prime UTR variant G/C;T snv
COLORECTAL CANCER, SUSCEPTIBILITY TO, 12
0.700 1.000 1 2019 2019
dbSNP: rs4246215
rs4246215
0.677 0.320 11 61796827 3 prime UTR variant G/C;T snv
CUI: C1281901
Disease: Fatty acid measurement
Fatty acid measurement
0.700 1.000 1 2015 2015
dbSNP: rs4246215
rs4246215
0.677 0.320 11 61796827 3 prime UTR variant G/C;T snv
CUI: C0009404
Disease: Colorectal Neoplasms
Colorectal Neoplasms
0.700 1.000 1 2019 2019
dbSNP: rs4246215
rs4246215
0.677 0.320 11 61796827 3 prime UTR variant G/C;T snv
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.700 1.000 1 2017 2017
dbSNP: rs4246215
rs4246215
0.677 0.320 11 61796827 3 prime UTR variant G/C;T snv
Malignant neoplasm of large intestine
0.700 1.000 1 2019 2019
dbSNP: rs4246215
rs4246215
0.677 0.320 11 61796827 3 prime UTR variant G/C;T snv
CUI: C0032181
Disease: Platelet Count measurement
Platelet Count measurement
0.800 1.000 1 2011 2011
dbSNP: rs4246215
rs4246215
0.677 0.320 11 61796827 3 prime UTR variant G/C;T snv
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
0.700 1.000 1 2019 2019
dbSNP: rs174541
rs174541
1.000 0.080 11 61798436 intron variant T/C snv 0.29
CUI: C0022661
Disease: Kidney Failure, Chronic
Kidney Failure, Chronic
0.700 1.000 1 2018 2018
dbSNP: rs174541
rs174541
1.000 0.080 11 61798436 intron variant T/C snv 0.29
CUI: C4049919
Disease: Insulin Sensitivity Measurement
Insulin Sensitivity Measurement
0.700 1.000 1 2013 2013
dbSNP: rs174541
rs174541
1.000 0.080 11 61798436 intron variant T/C snv 0.29
CUI: C1561643
Disease: Chronic Kidney Diseases
Chronic Kidney Diseases
0.700 1.000 1 2018 2018
dbSNP: rs174541
rs174541
1.000 0.080 11 61798436 intron variant T/C snv 0.29
CUI: C1281901
Disease: Fatty acid measurement
Fatty acid measurement
0.700 1.000 1 2015 2015
dbSNP: rs174544
rs174544
11 61800281 3 prime UTR variant C/A snv 0.25
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs174545
rs174545
1.000 0.080 11 61801834 3 prime UTR variant C/A;G snv 0.28
CUI: C0022661
Disease: Kidney Failure, Chronic
Kidney Failure, Chronic
0.700 1.000 1 2018 2018
dbSNP: rs174545
rs174545
1.000 0.080 11 61801834 3 prime UTR variant C/A;G snv 0.28
CUI: C1561643
Disease: Chronic Kidney Diseases
Chronic Kidney Diseases
0.700 1.000 1 2018 2018
dbSNP: rs174545
rs174545
1.000 0.080 11 61801834 3 prime UTR variant C/A;G snv 0.28
CUI: C1281901
Disease: Fatty acid measurement
Fatty acid measurement
0.700 1.000 1 2015 2015
dbSNP: rs174545
rs174545
1.000 0.080 11 61801834 3 prime UTR variant C/A;G snv 0.28
CUI: C2316832
Disease: Arachidonic acid measurement
Arachidonic acid measurement
0.700 1.000 1 2015 2015
dbSNP: rs174546
rs174546
0.807 0.200 11 61802358 3 prime UTR variant C/T snv 0.28
High density lipoprotein measurement
0.800 1.000 7 2010 2019
dbSNP: rs174546
rs174546
0.807 0.200 11 61802358 3 prime UTR variant C/T snv 0.28
Low density lipoprotein cholesterol measurement
0.800 1.000 6 2009 2019
dbSNP: rs174546
rs174546
0.807 0.200 11 61802358 3 prime UTR variant C/T snv 0.28
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.800 1.000 6 2008 2019