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: rs3181362
rs3181362
TNFSF8 ; DELEC1
1.000 0.040 9 114905163 intron variant T/C snv 0.21
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.700 1.000 1 2013 2013