rs2841498
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs2841498(A;A) |
| Make rs2841498(A;C) |
| Make rs2841498(C;C) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 9 |
| Position | 85315130 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2841498 |
| dbSNP (classic) | rs2841498 |
| ClinGen | rs2841498 |
| ebi | rs2841498 |
| HLI | rs2841498 |
| Exac | rs2841498 |
| Gnomad | rs2841498 |
| Varsome | rs2841498 |
| LitVar | rs2841498 |
| Map | rs2841498 |
| PheGenI | rs2841498 |
| Biobank | rs2841498 |
| 1000 genomes | rs2841498 |
| hgdp | rs2841498 |
| ensembl | rs2841498 |
| geneview | rs2841498 |
| scholar | rs2841498 |
| rs2841498 | |
| pharmgkb | rs2841498 |
| gwascentral | rs2841498 |
| openSNP | rs2841498 |
| 23andMe | rs2841498 |
| SNPshot | rs2841498 |
| SNPdbe | rs2841498 |
| MSV3d | rs2841498 |
| GWAS Ctlg | rs2841498 |
| GMAF | 0.1331 |
| Max Magnitude | 0 |
| ? | (A;A) (A;C) (C;C) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 20522523 ]
|
| Trait | Partial epilepsies |
| Title | Common genetic variation and susceptibility to partial epilepsies: a genome-wide association study |
| Risk Allele | |
| P-val | 0.000004 |
| Odds Ratio | None None |
