Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs211105
rs211105
TPH1
1.000 11 18033757 intron variant T/G snv 0.19
CUI: C0011991
Disease: Diarrhea
Diarrhea 		0.020 1.000 2 2015 2018
dbSNP: rs211105
rs211105
TPH1
1.000 11 18033757 intron variant T/G snv 0.19
CUI: C0740651
Disease: Abdominal symptom
Abdominal symptom 		0.010 1.000 1 2018 2018
dbSNP: rs211105
rs211105
TPH1
1.000 11 18033757 intron variant T/G snv 0.19
CUI: C0013395
Disease: Dyspepsia
Dyspepsia 		0.010 1.000 1 2018 2018
dbSNP: rs211105
rs211105
TPH1
1.000 11 18033757 intron variant T/G snv 0.19
CUI: C1262211
Disease: Diarrhoea predominant irritable bowel syndrome
Diarrhoea predominant irritable bowel syndrome 		0.010 1.000 1 2018 2018