rs4958847, IRGM

N. diseases: 8
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Crohn Disease
CUI: C0010346
Disease: Crohn Disease
1147 0.807 0.120 5 150860025 intron variant G/A snv 0.25 0.080 0.875 8 2008 2020
Ulcerative Colitis
CUI: C0009324
Disease: Ulcerative Colitis
827 0.807 0.120 5 150860025 intron variant G/A snv 0.25 0.030 0.667 3 2009 2013
Arthritis
CUI: C0003864
Disease: Arthritis
69 0.807 0.120 5 150860025 intron variant G/A snv 0.25 0.010 1.000 1 2020 2020
Inflammatory Bowel Diseases
CUI: C0021390
Disease: Inflammatory Bowel Diseases
605 0.807 0.120 5 150860025 intron variant G/A snv 0.25 0.010 1.000 1 2008 2008
Malignant neoplasm of stomach
CUI: C0024623
Disease: Malignant neoplasm of stomach
615 0.807 0.120 5 150860025 intron variant G/A snv 0.25 0.010 1.000 1 2012 2012
Non-alcoholic Fatty Liver Disease
CUI: C0400966
Disease: Non-alcoholic Fatty Liver Disease
222 0.807 0.120 5 150860025 intron variant G/A snv 0.25 0.010 1.000 1 2018 2018
pathologic fistula
CUI: C0016169
Disease: pathologic fistula
8 0.807 0.120 5 150860025 intron variant G/A snv 0.25 0.010 1.000 1 2009 2009
Stomach Carcinoma
CUI: C0699791
Disease: Stomach Carcinoma
652 0.807 0.120 5 150860025 intron variant G/A snv 0.25 0.010 1.000 1 2012 2012