rs211105, TPH1

N. diseases: 4
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 11 18033757 intron variant T/G snv 0.19 0.020 1.000 2 2015 2018
Abdominal symptom
CUI: C0740651
Disease: Abdominal symptom
3 1.000 11 18033757 intron variant T/G snv 0.19 0.010 1.000 1 2018 2018
Diarrhoea predominant irritable bowel syndrome
CUI: C1262211
Disease: Diarrhoea predominant irritable bowel syndrome
8 1.000 11 18033757 intron variant T/G snv 0.19 0.010 1.000 1 2018 2018
Dyspepsia
CUI: C0013395
Disease: Dyspepsia
5 1.000 11 18033757 intron variant T/G snv 0.19 0.010 1.000 1 2018 2018