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.
