rs2076756, NOD2

N. diseases: 5
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.
pathologic fistula
CUI: C0016169
Disease: pathologic fistula
8 0.882 0.040 16 50722970 intron variant A/G snv 0.17 0.010 1.000 1 2010 2010
Pouchitis
CUI: C0376620
Disease: Pouchitis
10 0.882 0.040 16 50722970 intron variant A/G snv 0.17 0.010 1.000 1 2017 2017
Inflammatory Bowel Diseases
CUI: C0021390
Disease: Inflammatory Bowel Diseases
605 0.882 0.040 16 50722970 intron variant A/G snv 0.17 0.820 1.000 3 2006 2017
Ulcerative Colitis
CUI: C0009324
Disease: Ulcerative Colitis
827 0.882 0.040 16 50722970 intron variant A/G snv 0.17 0.010 1.000 1 2010 2010
Crohn Disease
CUI: C0010346
Disease: Crohn Disease
1147 0.882 0.040 16 50722970 intron variant A/G snv 0.17 0.830 1.000 9 2007 2019