rs77905

minus

Geno	Mag	Summary
(T;T)	0	common in clinvar

Make rs77905(C;C)

Make rs77905(C;T)

Reference

GRCh38 38.1/141

Chromosome

9

Position

133652975

Gene

DBH

is a	snp
is	mentioned by
dbSNP	rs77905
dbSNP (classic)	rs77905
ClinGen	rs77905
ebi	rs77905
HLI	rs77905
Exac	rs77905
Gnomad	rs77905
Varsome	rs77905
LitVar	rs77905
Map	rs77905
PheGenI	rs77905
Biobank	rs77905
1000 genomes	rs77905
hgdp	rs77905
ensembl	rs77905
geneview	rs77905
scholar	rs77905
google	rs77905
pharmgkb	rs77905
gwascentral	rs77905
openSNP	rs77905
23andMe	rs77905
SNPshot	rs77905
SNPdbe	rs77905
MSV3d	rs77905
GWAS Ctlg	rs77905

GMAF

0.3545

Max Magnitude

0

?

(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 18486967 ] 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 19673036 ] 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,