rs10496964
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs10496964(C;C) |
| Make rs10496964(C;T) |
| Make rs10496964(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 2 |
| Position | 144602342 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs10496964 |
| dbSNP (classic) | rs10496964 |
| ClinGen | rs10496964 |
| ebi | rs10496964 |
| HLI | rs10496964 |
| Exac | rs10496964 |
| Gnomad | rs10496964 |
| Varsome | rs10496964 |
| LitVar | rs10496964 |
| Map | rs10496964 |
| PheGenI | rs10496964 |
| Biobank | rs10496964 |
| 1000 genomes | rs10496964 |
| hgdp | rs10496964 |
| ensembl | rs10496964 |
| geneview | rs10496964 |
| scholar | rs10496964 |
| rs10496964 | |
| pharmgkb | rs10496964 |
| gwascentral | rs10496964 |
| openSNP | rs10496964 |
| 23andMe | rs10496964 |
| SNPshot | rs10496964 |
| SNPdbe | rs10496964 |
| MSV3d | rs10496964 |
| GWAS Ctlg | rs10496964 |
| GMAF | 0.124 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 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 | C |
| P-val | 9E-9 |
| Odds Ratio | 1.47 [1.28-1.67] |
