rs2076756, NOD2

N. diseases: 2
Source: GWASDB ×
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
332 0.882 0.040 16 50722970 intron variant A/G snv 0.17 0.830 1.000 6 2007 2019
Inflammatory Bowel Diseases
CUI: C0021390
Disease: Inflammatory Bowel Diseases
122 0.882 0.040 16 50722970 intron variant A/G snv 0.17 0.820 1.000 1 2006 2017