Source: GWASDB

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: rs2413583
rs2413583 		0.925 0.040 22 39263768 intron variant C/T snv 0.19
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases 		0.800 1.000 1 2012 2017
dbSNP: rs2413583
rs2413583 		0.925 0.040 22 39263768 intron variant C/T snv 0.19
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.800 1.000 1 2010 2017