Source: GWASCAT

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: rs694739
rs694739
0.763 0.320 11 64329761 upstream gene variant A/G snv 0.28
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.800 1.000 1 2010 2010
dbSNP: rs694739
rs694739
0.763 0.320 11 64329761 upstream gene variant A/G snv 0.28
CUI: C0002171
Disease: Alopecia Areata
Alopecia Areata
0.800 1.000 1 2010 2010
dbSNP: rs694739
rs694739
0.763 0.320 11 64329761 upstream gene variant A/G snv 0.28
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis
0.800 1.000 1 2012 2012
dbSNP: rs694739
rs694739
0.763 0.320 11 64329761 upstream gene variant A/G snv 0.28
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis
0.700 1.000 1 2013 2013
dbSNP: rs694739
rs694739
0.763 0.320 11 64329761 upstream gene variant A/G snv 0.28
CUI: C0036202
Disease: Sarcoidosis
Sarcoidosis
0.700 1.000 1 2015 2015
dbSNP: rs694739
rs694739
0.763 0.320 11 64329761 upstream gene variant A/G snv 0.28
CUI: C0263361
Disease: Psoriasis vulgaris
Psoriasis vulgaris
0.700 1.000 1 2015 2015