rs12466358
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs12466358(G;G) |
| Make rs12466358(G;T) |
| Make rs12466358(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 2 |
| Position | 232532815 |
| Gene | CHRND |
| is a | snp |
| is | mentioned by |
| dbSNP | rs12466358 |
| dbSNP (classic) | rs12466358 |
| ClinGen | rs12466358 |
| ebi | rs12466358 |
| HLI | rs12466358 |
| Exac | rs12466358 |
| Gnomad | rs12466358 |
| Varsome | rs12466358 |
| LitVar | rs12466358 |
| Map | rs12466358 |
| PheGenI | rs12466358 |
| Biobank | rs12466358 |
| 1000 genomes | rs12466358 |
| hgdp | rs12466358 |
| ensembl | rs12466358 |
| geneview | rs12466358 |
| scholar | rs12466358 |
| rs12466358 | |
| pharmgkb | rs12466358 |
| gwascentral | rs12466358 |
| openSNP | rs12466358 |
| 23andMe | rs12466358 |
| SNPshot | rs12466358 |
| SNPdbe | rs12466358 |
| MSV3d | rs12466358 |
| GWAS Ctlg | rs12466358 |
| GMAF | 0.2704 |
| Max Magnitude | 0 |
| ? | (G;G) (G;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 20840187
] Peer smoking and the nicotinic receptor genes: an examination of genetic and environmental risks for nicotine dependence
[PMID 19259974] Multiple distinct risk loci for nicotine dependence identified by dense coverage of the complete family of nicotinic receptor subunit (CHRN) genes.
