Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 121278
Gene Symbol: TPH2
TPH2 		0.020 GeneticVariation disease BEFREE Genetic variation at the TPH2 gene appeared to affect impulsivity which, in turn, might predispose to the SV phenotype. 23239044 2013
Entrez Id: 121278
Gene Symbol: TPH2
TPH2 		0.020 GeneticVariation disease BEFREE The meta-analysis revealed that the tryptophan hydroxylase 2 polymorphism rs1473473 was associated with a higher risk for AN, EDs characterized by SV and for the combined group. 20946355 2011
Entrez Id: 627
Gene Symbol: BDNF
BDNF 		0.010 Biomarker disease BEFREE We investigated the association of 25 single nucleotide polymorphisms (SNPs), capturing 71-91% of the common variance in candidate genes, stathmin (STMN1), serotonin receptor 1D (HTR1D), tryptophan hydroxylase 2 (TPH2) and brain-derived neurotrophic factor (BDNF), with AN and EDs characterized by regular SV. 20946355 2011
Entrez Id: 3925
Gene Symbol: STMN1
STMN1 		0.010 GeneticVariation disease BEFREE We investigated the association of 25 single nucleotide polymorphisms (SNPs), capturing 71-91% of the common variance in candidate genes, stathmin (STMN1), serotonin receptor 1D (HTR1D), tryptophan hydroxylase 2 (TPH2) and brain-derived neurotrophic factor (BDNF), with AN and EDs characterized by regular SV. 20946355 2011
Entrez Id: 3352
Gene Symbol: HTR1D
HTR1D 		0.010 GeneticVariation disease BEFREE We investigated the association of 25 single nucleotide polymorphisms (SNPs), capturing 71-91% of the common variance in candidate genes, stathmin (STMN1), serotonin receptor 1D (HTR1D), tryptophan hydroxylase 2 (TPH2) and brain-derived neurotrophic factor (BDNF), with AN and EDs characterized by regular SV. 20946355 2011