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: rs2006996
rs2006996 		0.882 0.080 9 114830358 regulatory region variant T/C snv 7.2E-02
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.800 1.000 1 2011 2013
dbSNP: rs2006996
rs2006996 		0.882 0.080 9 114830358 regulatory region variant T/C snv 7.2E-02
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases 		0.700 1.000 1 2011 2011
dbSNP: rs2006996
rs2006996 		0.882 0.080 9 114830358 regulatory region variant T/C snv 7.2E-02
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis 		0.700 1.000 1 2012 2012