Source: GWASCAT

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: rs2076756
rs2076756
NOD2
0.882 0.040 16 50722970 intron variant A/G snv 0.17
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.830 1.000 5 2007 2019
dbSNP: rs2076756
rs2076756
NOD2
0.882 0.040 16 50722970 intron variant A/G snv 0.17
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases 		0.820 1.000 1 2006 2017