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rs11042950

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs11042950(A;A)
Make rs11042950(A;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position2168488
GeneTH
is asnp
is mentioned by
dbSNPrs11042950
ebirs11042950
HLIrs11042950
Exacrs11042950
Varsomers11042950
Maprs11042950
PheGenIrs11042950
hapmaprs11042950
1000 genomesrs11042950
hgdprs11042950
ensemblrs11042950
gopubmedrs11042950
geneviewrs11042950
scholarrs11042950
googlers11042950
pharmgkbrs11042950
gwascentralrs11042950
openSNPrs11042950
23andMers11042950
23andMe allrs11042950
SNP Nexus

SNPshotrs11042950
SNPdbers11042950
MSV3drs11042950
GWAS Ctlgrs11042950
GMAF0.002755
Max Magnitude0
? (A;A) (A;G) (G;G) 28

[PMID 24275212] The role of tyrosine hydroxylase gene variants in suicide attempt in schizophrenia


ClinVar
Risk rs11042950(A;A)
Alt rs11042950(A;A)
Reference rs11042950(G;G)
Significance Non-pathogenic
Disease Dystonia
Variation info
Gene TH
CLNDBN Dystonia
Reversed 1
HGVS NC_000011.9:g.2189718C>T
CLNSRC
CLNACC RCV000229985.1,