Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs6784820
rs6784820
1.000 0.040 3 49413431 intron variant A/G snv 0.40
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
Digestive System Diseases 0.700 1.000 1 2008 2008
dbSNP: rs6997
rs6997
1.000 0.040 3 49416401 3 prime UTR variant C/T snv 0.30
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
Digestive System Diseases 0.700 1.000 1 2007 2007