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rs11178998

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs11178998(A;G)
Make rs11178998(G;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position71938935
GeneTPH2
is asnp
is mentioned by
dbSNPrs11178998
dbSNP (classic)rs11178998
ClinGenrs11178998
ebirs11178998
HLIrs11178998
Exacrs11178998
Gnomadrs11178998
Varsomers11178998
LitVarrs11178998
Maprs11178998
PheGenIrs11178998
Biobankrs11178998
1000 genomesrs11178998
hgdprs11178998
ensemblrs11178998
geneviewrs11178998
scholarrs11178998
googlers11178998
pharmgkbrs11178998
gwascentralrs11178998
openSNPrs11178998
23andMers11178998
SNPshotrs11178998
SNPdbers11178998
MSV3drs11178998
GWAS Ctlgrs11178998
GMAF0.08724
Max Magnitude0
OMIM607478
DescTRYPTOPHAN HYDROXYLASE 2; TPH2
Variant
Relatedalso
OMIM125480
Desc
Variant
Relatedalso

[PMID 18797398] Investigation of the tryptophan hydroxylase 2 gene in bipolar I disorder in the Romanian population. [PMID 22655589] Investigation of tryptophan hydroxylase 2 (TPH2) in schizophrenia and in the response to antipsychotics.


ClinVar
Risk rs11178998(G;G)
Alt rs11178998(G;G)
Reference Rs11178998(A;A)
Significance Probable-non-pathogenic
Disease Tryptophan 5-monooxygenase deficiency
Variation info
Gene TPH2
CLNDBN Tryptophan 5-monooxygenase deficiency
Reversed 0
HGVS NC_000012.11:g.72332715A>G
CLNSRC
CLNACC RCV000387456.1,