Source: ALL

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: rs13361189
rs13361189
0.752 0.240 5 150843825 upstream gene variant T/C snv 0.21
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.850 1.000 7 2007 2015
dbSNP: rs13361189
rs13361189
0.752 0.240 5 150843825 upstream gene variant T/C snv 0.21
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis
0.020 0.500 2 2009 2013
dbSNP: rs13361189
rs13361189
0.752 0.240 5 150843825 upstream gene variant T/C snv 0.21
CUI: C0400966
Disease: Non-alcoholic Fatty Liver Disease
Non-alcoholic Fatty Liver Disease
0.020 1.000 2 2018 2019
dbSNP: rs13361189
rs13361189
0.752 0.240 5 150843825 upstream gene variant T/C snv 0.21
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach
0.010 < 0.001 1 2012 2012
dbSNP: rs13361189
rs13361189
0.752 0.240 5 150843825 upstream gene variant T/C snv 0.21
CUI: C0018213
Disease: Graves Disease
Graves Disease
0.010 1.000 1 2018 2018
dbSNP: rs13361189
rs13361189
0.752 0.240 5 150843825 upstream gene variant T/C snv 0.21
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.010 < 0.001 1 2012 2012
dbSNP: rs13361189
rs13361189
0.752 0.240 5 150843825 upstream gene variant T/C snv 0.21
CUI: C0021831
Disease: Intestinal Diseases
Intestinal Diseases
0.010 1.000 1 2015 2015
dbSNP: rs13361189
rs13361189
0.752 0.240 5 150843825 upstream gene variant T/C snv 0.21
CUI: C0017638
Disease: Glioma
Glioma
0.010 1.000 1 2014 2014
dbSNP: rs13361189
rs13361189
0.752 0.240 5 150843825 upstream gene variant T/C snv 0.21
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases
0.010 1.000 1 2008 2008
dbSNP: rs13361189
rs13361189
0.752 0.240 5 150843825 upstream gene variant T/C snv 0.21
CUI: C0015695
Disease: Fatty Liver
Fatty Liver
0.010 < 0.001 1 2019 2019
dbSNP: rs13361189
rs13361189
0.752 0.240 5 150843825 upstream gene variant T/C snv 0.21
CUI: C0041296
Disease: Tuberculosis
Tuberculosis
0.010 1.000 1 2016 2016
dbSNP: rs13361189
rs13361189
0.752 0.240 5 150843825 upstream gene variant T/C snv 0.21
CUI: C0020875
Disease: Ileal Diseases
Ileal Diseases
0.010 1.000 1 2015 2015
dbSNP: rs13361189
rs13361189
0.752 0.240 5 150843825 upstream gene variant T/C snv 0.21
CUI: C2711227
Disease: Steatohepatitis
Steatohepatitis
0.010 < 0.001 1 2019 2019