rs4952
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs4952(C;C) |
Make rs4952(C;T) |
Make rs4952(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 8 |
Position | 42731922 |
Gene | CHRNB3 |
is a | snp |
is | mentioned by |
dbSNP | rs4952 |
dbSNP (classic) | rs4952 |
ClinGen | rs4952 |
ebi | rs4952 |
HLI | rs4952 |
Exac | rs4952 |
Gnomad | rs4952 |
Varsome | rs4952 |
LitVar | rs4952 |
Map | rs4952 |
PheGenI | rs4952 |
Biobank | rs4952 |
1000 genomes | rs4952 |
hgdp | rs4952 |
ensembl | rs4952 |
geneview | rs4952 |
scholar | rs4952 |
rs4952 | |
pharmgkb | rs4952 |
gwascentral | rs4952 |
openSNP | rs4952 |
23andMe | rs4952 |
SNPshot | rs4952 |
SNPdbe | rs4952 |
MSV3d | rs4952 |
GWAS Ctlg | rs4952 |
GMAF | 0.01928 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 24401102] Multiple distinct CHRNB3-CHRNA6 variants are genetic risk factors for nicotine dependence in African Americans and European Americans
[PMID 17135278] Cholinergic nicotinic receptor genes implicated in a nicotine dependence association study targeting 348 candidate genes with 3713 SNPs.
[PMID 18571741] Genetic variability in nicotinic acetylcholine receptors and nicotine addiction: converging evidence from human and animal research.
[PMID 19029397] Nicotinic receptor gene variants influence susceptibility to heavy smoking.
[PMID 21191315] Genetic association of bipolar disorder with the beta(3) nicotinic receptor subunit gene.