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: rs10489276
rs10489276 		1.000 0.040 1 172893799 intron variant C/T snv 0.31
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.700 1.000 1 2008 2008