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rs11179027

From SNPedia

Orientationplus
Stabilizedplus
Make rs11179027(C;C)
Make rs11179027(C;G)
Make rs11179027(G;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position71983532
GeneTPH2
is asnp
is mentioned by
dbSNPrs11179027
ebirs11179027
HLIrs11179027
Exacrs11179027
Varsomers11179027
Maprs11179027
PheGenIrs11179027
hapmaprs11179027
1000 genomesrs11179027
hgdprs11179027
ensemblrs11179027
gopubmedrs11179027
geneviewrs11179027
scholarrs11179027
googlers11179027
pharmgkbrs11179027
gwascentralrs11179027
openSNPrs11179027
23andMers11179027
23andMe allrs11179027
SNP Nexus

SNPshotrs11179027
SNPdbers11179027
MSV3drs11179027
GWAS Ctlgrs11179027
GMAF0.3315
Max Magnitude
? (C;C) (C;G) (G;G) 28

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


[PMID 23337130] Common genetic background in anorexia nervosa and obsessive compulsive disorder: preliminary results from an association study.


[PMID 23461725] Association between TPH2 gene polymorphisms and attention deficit hyperactivity disorder in Korean children.