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: rs1476273292
rs1476273292
1.000 0.040 12 98712328 missense variant G/A snv 4.0E-06
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
Digestive System Diseases 0.010 1.000 1 2002 2002
dbSNP: rs746482334
rs746482334
1.000 0.040 12 98732507 missense variant A/G snv 4.0E-06
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
Digestive System Diseases 0.010 < 0.001 1 2003 2003