Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs120074176
rs120074176
Entrez Id: 121278
Gene Symbol: TPH2
TPH2
CUI: C2751802
Disease:
ATTENTION DEFICIT-HYPERACTIVITY DISORDER, SUSCEPTIBILITY TO, 7
0.800 GeneticVariation UNIPROT A loss-of-function mutation in tryptophan hydroxylase 2 segregating with attention-deficit/hyperactivity disorder. 18347598 2008
dbSNP: rs120074176
rs120074176
Entrez Id: 121278
Gene Symbol: TPH2
TPH2
CUI: C2751802
Disease:
ATTENTION DEFICIT-HYPERACTIVITY DISORDER, SUSCEPTIBILITY TO, 7
T 0.800 SusceptibilityMutation CLINVAR