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rs4469933

From SNPedia

Orientationplus
Stabilizedplus
Make rs4469933(C;C)
Make rs4469933(C;T)
Make rs4469933(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position72020937
GeneTPH2
is asnp
is mentioned by
dbSNPrs4469933
ebirs4469933
HLIrs4469933
Exacrs4469933
Varsomers4469933
Maprs4469933
PheGenIrs4469933
hapmaprs4469933
1000 genomesrs4469933
hgdprs4469933
ensemblrs4469933
gopubmedrs4469933
geneviewrs4469933
scholarrs4469933
googlers4469933
pharmgkbrs4469933
gwascentralrs4469933
openSNPrs4469933
23andMers4469933
23andMe allrs4469933
SNP Nexus

SNPshotrs4469933
SNPdbers4469933
MSV3drs4469933
GWAS Ctlgrs4469933
GMAF0.4839
Max Magnitude
? (C;C) (C;T) (T;T) 28

[PMID 21396719] Influence of TPH2 variants on diagnosis and response to treatment in patients with major depression, bipolar disorder and schizophrenia