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: rs17293632
rs17293632
0.763 0.240 15 67150258 intron variant C/T snv 0.17
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases
0.800 1.000 1 2012 2017
dbSNP: rs17293632
rs17293632
0.763 0.240 15 67150258 intron variant C/T snv 0.17
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.800 1.000 1 2010 2017
dbSNP: rs17293632
rs17293632
0.763 0.240 15 67150258 intron variant C/T snv 0.17
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction
0.700 1.000 1 2013 2013