FOXP2, forkhead box P2, 93986

N. diseases: 165; N. variants: 32
Disease: Hallucinations, Auditory ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2396753
rs2396753
Entrez Id: 93986
Gene Symbol: FOXP2
FOXP2
CUI: C0233762
Disease:
Hallucinations, Auditory 		0.010 GeneticVariation BEFREE Statistically significant differences in the genotype (P=0.007) and allele frequencies (P=0.0027) between schizophrenic patients with auditory hallucinations and controls were found in the single nucleotide polymorphism rs2396753. 16538183 2006