rs1881492
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs1881492(G;G) |
| Make rs1881492(G;T) |
| Make rs1881492(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 2 |
| Position | 232542288 |
| Gene | CHRNG |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1881492 |
| dbSNP (classic) | rs1881492 |
| ClinGen | rs1881492 |
| ebi | rs1881492 |
| HLI | rs1881492 |
| Exac | rs1881492 |
| Gnomad | rs1881492 |
| Varsome | rs1881492 |
| LitVar | rs1881492 |
| Map | rs1881492 |
| PheGenI | rs1881492 |
| Biobank | rs1881492 |
| 1000 genomes | rs1881492 |
| hgdp | rs1881492 |
| ensembl | rs1881492 |
| geneview | rs1881492 |
| scholar | rs1881492 |
| rs1881492 | |
| pharmgkb | rs1881492 |
| gwascentral | rs1881492 |
| openSNP | rs1881492 |
| 23andMe | rs1881492 |
| SNPshot | rs1881492 |
| SNPdbe | rs1881492 |
| MSV3d | rs1881492 |
| GWAS Ctlg | rs1881492 |
| GMAF | 0.1887 |
| Max Magnitude | 0 |
| ? | (G;G) (G;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 23396134 ]
|
| Trait | Refractive error |
| Title | Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia. |
| Risk Allele | T |
| P-val | 5E-11 |
| Odds Ratio | .14 [0.098-0.18] unit decrease |
[PMID 19259974] Multiple distinct risk loci for nicotine dependence identified by dense coverage of the complete family of nicotinic receptor subunit (CHRN) genes.
