rs771184127, NOD2

N. diseases: 9
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 0.790 0.200 16 50710807 missense variant G/A snv 1.2E-05 2.1E-05 0.100 0.917 12 2004 2017
Inflammatory Bowel Diseases
CUI: C0021390
Disease: Inflammatory Bowel Diseases
605 0.790 0.200 16 50710807 missense variant G/A snv 1.2E-05 2.1E-05 0.060 1.000 6 2004 2017
Ulcerative Colitis
CUI: C0009324
Disease: Ulcerative Colitis
827 0.790 0.200 16 50710807 missense variant G/A snv 1.2E-05 2.1E-05 0.050 1.000 5 2004 2017
Arthritis
CUI: C0003864
Disease: Arthritis
69 0.790 0.200 16 50710807 missense variant G/A snv 1.2E-05 2.1E-05 0.010 1.000 1 2017 2017
Gastritis
CUI: C0017152
Disease: Gastritis
21 0.790 0.200 16 50710807 missense variant G/A snv 1.2E-05 2.1E-05 0.010 1.000 1 2010 2010
Helicobacter pylori (H. pylori) infection in conditions classified elsewhere and of unspecified site
CUI: C0374997
Disease: Helicobacter pylori (H. pylori) infection in conditions classified elsewhere and of unspecified site
24 0.790 0.200 16 50710807 missense variant G/A snv 1.2E-05 2.1E-05 0.010 1 2007 2007
HELLP Syndrome
CUI: C0162739
Disease: HELLP Syndrome
10 0.790 0.200 16 50710807 missense variant G/A snv 1.2E-05 2.1E-05 0.010 1.000 1 2008 2008
Hereditary hemochromatosis
CUI: C0392514
Disease: Hereditary hemochromatosis
56 0.790 0.200 16 50710807 missense variant G/A snv 1.2E-05 2.1E-05 0.010 1.000 1 2010 2010
Intestinal metaplasia
CUI: C0334037
Disease: Intestinal metaplasia
24 0.790 0.200 16 50710807 missense variant G/A snv 1.2E-05 2.1E-05 0.010 1 2007 2007