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: rs2302759
rs2302759
CYLD ; LOC105371251
1.000 0.040 16 50793690 intron variant A/C;G snv 4.0E-06; 0.79
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.700 1.000 1 2007 2007