rs12059546
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs12059546(A;A) |
| Make rs12059546(A;G) |
| Make rs12059546(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 239806797 |
| Gene | CHRM3 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs12059546 |
| dbSNP (classic) | rs12059546 |
| ClinGen | rs12059546 |
| ebi | rs12059546 |
| HLI | rs12059546 |
| Exac | rs12059546 |
| Gnomad | rs12059546 |
| Varsome | rs12059546 |
| LitVar | rs12059546 |
| Map | rs12059546 |
| PheGenI | rs12059546 |
| Biobank | rs12059546 |
| 1000 genomes | rs12059546 |
| hgdp | rs12059546 |
| ensembl | rs12059546 |
| geneview | rs12059546 |
| scholar | rs12059546 |
| rs12059546 | |
| pharmgkb | rs12059546 |
| gwascentral | rs12059546 |
| openSNP | rs12059546 |
| 23andMe | rs12059546 |
| SNPshot | rs12059546 |
| SNPdbe | rs12059546 |
| MSV3d | rs12059546 |
| GWAS Ctlg | rs12059546 |
| GMAF | 0.3205 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 22949513] |
| Trait | Epilepsy (generalized) |
| Title | Genome-wide association analysis of genetic generalized epilepsies implicates susceptibility loci at 1q43, 2p16.1, 2q22.3 and 17q21.32 |
| Risk Allele | G |
| P-val | 4E-8 |
| Odds Ratio | 1.42 [1.26-1.61] |
