Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs120074176
rs120074176
TPH2
0.800 GeneticVariation UNIPROT A loss-of-function mutation in tryptophan hydroxylase 2 segregating with attention-deficit/hyperactivity disorder. 18347598

2008
dbSNP: rs120074176
rs120074176
TPH2
T 0.800 SusceptibilityMutation CLINVAR