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: rs7746082
rs7746082 		0.851 0.160 6 105987394 regulatory region variant G/A;C snv
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.810 1.000 1 2008 2017
dbSNP: rs7746082
rs7746082 		0.851 0.160 6 105987394 regulatory region variant G/A;C snv
CUI: C0004096
Disease: Asthma
Asthma 		0.700 1.000 1 2011 2011
dbSNP: rs7746082
rs7746082 		0.851 0.160 6 105987394 regulatory region variant G/A;C snv
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		0.700 1.000 1 2011 2011