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: rs4246905
rs4246905
0.716 0.400 9 114790969 missense variant T/A;C snv 0.76
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases
Digestive System Diseases 0.800 1.000 1 2012 2012
dbSNP: rs6478109
rs6478109
0.752 0.320 9 114806486 upstream gene variant A/G snv 0.74
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases
Digestive System Diseases 0.800 1.000 1 2008 2008
dbSNP: rs7848647
rs7848647
0.732 0.320 9 114806766 upstream gene variant T/C snv 0.74
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases
Digestive System Diseases 0.710 1.000 2 2015 2018
dbSNP: rs10114470
rs10114470
0.882 0.080 9 114785492 3 prime UTR variant T/A;C snv
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases
Digestive System Diseases 0.010 1.000 1 2017 2017
dbSNP: rs3810936
rs3810936
0.742 0.320 9 114790605 synonymous variant T/C snv 0.71 0.75
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases
Digestive System Diseases 0.010 1.000 1 2018 2018
dbSNP: rs6478108
rs6478108
0.763 0.200 9 114796423 intron variant C/T snv 0.73
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases
Digestive System Diseases 0.010 1.000 1 2018 2018