rs10474485, CRHBP

N. diseases: 2
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Diarrhea
CUI: C0011991
Disease: Diarrhea
63 1.000 0.040 5 76975028 intron variant C/A snv 0.26 0.010 1.000 1 2016 2016
Irritable Bowel Syndrome
CUI: C0022104
Disease: Irritable Bowel Syndrome
52 1.000 0.040 5 76975028 intron variant C/A snv 0.26 0.010 1.000 1 2016 2016