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: rs3779250
rs3779250
0.925 0.080 7 30654644 intron variant C/T snv 0.48
CUI: C0022104
Disease: Irritable Bowel Syndrome
Irritable Bowel Syndrome
Digestive System Diseases 0.010 1.000 1 2016 2016
dbSNP: rs4722999
rs4722999
0.851 0.080 7 30654159 intron variant C/T snv 0.67
CUI: C0022104
Disease: Irritable Bowel Syndrome
Irritable Bowel Syndrome
Digestive System Diseases 0.010 1.000 1 2016 2016