rs569207
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs569207(A;A) |
| Make rs569207(A;G) |
| Make rs569207(G;G) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 15 |
| Position | 78580777 |
| Gene | CHRNA5 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs569207 |
| dbSNP (classic) | rs569207 |
| ClinGen | rs569207 |
| ebi | rs569207 |
| HLI | rs569207 |
| Exac | rs569207 |
| Gnomad | rs569207 |
| Varsome | rs569207 |
| LitVar | rs569207 |
| Map | rs569207 |
| PheGenI | rs569207 |
| Biobank | rs569207 |
| 1000 genomes | rs569207 |
| hgdp | rs569207 |
| ensembl | rs569207 |
| geneview | rs569207 |
| scholar | rs569207 |
| rs569207 | |
| pharmgkb | rs569207 |
| gwascentral | rs569207 |
| openSNP | rs569207 |
| 23andMe | rs569207 |
| SNPshot | rs569207 |
| SNPdbe | rs569207 |
| MSV3d | rs569207 |
| GWAS Ctlg | rs569207 |
| GMAF | 0.3618 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 18519524
] Variants in nicotinic receptors and risk for nicotine dependence.
[PMID 19029397] Nicotinic receptor gene variants influence susceptibility to heavy smoking.
[PMID 19436041] Human neuronal acetylcholine receptor A5-A3-B4 haplotypes are associated with multiple nicotine dependence phenotypes.
[PMID 19443489] Risk for nicotine dependence and lung cancer is conferred by mRNA expression levels and amino acid change in CHRNA5.
[PMID 20700436] Multiple independent loci at chromosome 15q25.1 affect smoking quantity: a meta-analysis and comparison with lung cancer and COPD.
[PMID 20808433] Associations of variants in CHRNA5/A3/B4 gene cluster with smoking behaviors in a Korean population.
