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rs77905

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs77905(C;C)
Make rs77905(C;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position133652975
GeneDBH
is asnp
is mentioned by
dbSNPrs77905
dbSNP (classic)rs77905
ClinGenrs77905
ebirs77905
HLIrs77905
Exacrs77905
Gnomadrs77905
Varsomers77905
LitVarrs77905
Maprs77905
PheGenIrs77905
Biobankrs77905
1000 genomesrs77905
hgdprs77905
ensemblrs77905
geneviewrs77905
scholarrs77905
googlers77905
pharmgkbrs77905
gwascentralrs77905
openSNPrs77905
23andMers77905
SNPshotrs77905
SNPdbers77905
MSV3drs77905
GWAS Ctlgrs77905
GMAF0.3545
Max Magnitude0
? (C;C) (C;T) (T;T) 28


Genetic variation in the dopamine pathway and smoking cessation.[PMID 18781857]


[PMID 20350135] Prospective association of dopamine-related polymorphisms with smoking cessation in general care


[PMID 16272956] CYP2A6, MAOA, DBH, DRD4, and 5HT2A genotypes, smoking behaviour and cotinine levels in 1518 UK adolescents.


[PMID 18486967OA-icon.png] A community-based study of cigarette smoking behavior in relation to variation in three genes involved in dopamine metabolism: Catechol-O-methyltransferase (COMT), dopamine beta-hydroxylase (DBH) and monoamine oxidase-A (MAO-A).


[PMID 19673036OA-icon.png] Association of tagging single nucleotide polymorphisms on 8 candidate genes in dopaminergic pathway with schizophrenia in Croatian population.


ClinVar
Risk rs77905(C;C)
Alt rs77905(C;C)
Reference Rs77905(T;T)
Significance Non-pathogenic
Disease Dopamine beta hydroxylase deficiency
Variation info
Gene DBH
CLNDBN Dopamine beta hydroxylase deficiency
Reversed 1
HGVS NC_000009.11:g.136518097A>G
CLNSRC
CLNACC RCV000402576.1,