rs346291
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs346291(C;C) |
| Make rs346291(C;T) |
| Make rs346291(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 6 |
| Position | 79855119 |
| Gene | C6orf7 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs346291 |
| dbSNP (classic) | rs346291 |
| ClinGen | rs346291 |
| ebi | rs346291 |
| HLI | rs346291 |
| Exac | rs346291 |
| Gnomad | rs346291 |
| Varsome | rs346291 |
| LitVar | rs346291 |
| Map | rs346291 |
| PheGenI | rs346291 |
| Biobank | rs346291 |
| 1000 genomes | rs346291 |
| hgdp | rs346291 |
| ensembl | rs346291 |
| geneview | rs346291 |
| scholar | rs346291 |
| rs346291 | |
| pharmgkb | rs346291 |
| gwascentral | rs346291 |
| openSNP | rs346291 |
| 23andMe | rs346291 |
| SNPshot | rs346291 |
| SNPdbe | rs346291 |
| MSV3d | rs346291 |
| GWAS Ctlg | rs346291 |
| GMAF | 0.3742 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 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 | 3E-7 |
| Odds Ratio | 1.20 [1.12-1.30] |
