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rs4448731

From SNPedia

Orientationplus
Stabilizedplus
Make rs4448731(C;C)
Make rs4448731(C;T)
Make rs4448731(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position71935326
is asnp
is mentioned by
dbSNPrs4448731
ebirs4448731
HLIrs4448731
Exacrs4448731
Varsomers4448731
Maprs4448731
PheGenIrs4448731
hapmaprs4448731
1000 genomesrs4448731
hgdprs4448731
ensemblrs4448731
gopubmedrs4448731
geneviewrs4448731
scholarrs4448731
googlers4448731
pharmgkbrs4448731
gwascentralrs4448731
openSNPrs4448731
23andMers4448731
23andMe allrs4448731
SNP Nexus

SNPshotrs4448731
SNPdbers4448731
MSV3drs4448731
GWAS Ctlgrs4448731
GMAF0.3848
Max Magnitude
? (C;C) (C;T) (T;T) 28

[PMID 19800079] Association of polymorphisms of the tryptophan hydroxylase 2 gene with risk for bipolar disorder or suicidal behavior


[PMID 17217922] Effect of tryptophan hydroxylase-2 gene variants on suicide risk in major depression.


[PMID 21085052] Association study of tryptophan hydroxylase 2 gene polymorphisms in bipolar disorder patients with panic disorder comorbidity.


[PMID 21172166OA-icon.png] Pharmacogenetics of antidepressant response.


[PMID 21412658] Associations between polymorphic variants of the tryptophan hydroxylase 2 gene and obsessive-compulsive disorder.


[PMID 22392150] Common variants in the TPH2 promoter confer susceptibility to paranoid schizophrenia.