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: rs1248696
rs1248696
0.807 0.080 10 77856847 missense variant T/A;C snv 0.93
CUI: C2931133
Disease: Pediatric Crohn's disease
Pediatric Crohn's disease
Digestive System Diseases 0.010 1.000 1 2007 2007
dbSNP: rs2165047
rs2165047
1.000 0.040 10 77791882 3 prime UTR variant C/T snv 0.26
CUI: C2931133
Disease: Pediatric Crohn's disease
Pediatric Crohn's disease
Digestive System Diseases 0.010 1.000 1 2007 2007