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: rs56399423
rs56399423
5 132336964 intron variant T/C snv 0.28
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases
Digestive System Diseases 0.700 1.000 1 2015 2015
dbSNP: rs1050152
rs1050152
0.776 0.480 5 132340627 missense variant C/T snv 0.29 0.28
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases
Digestive System Diseases 0.040 1.000 4 2006 2017
dbSNP: rs272879
rs272879
0.882 0.040 5 132334853 synonymous variant C/A;G;T snv 4.0E-06; 0.57
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases
Digestive System Diseases 0.010 < 0.001 1 2010 2010