rs992353
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs992353(A;A) |
| Make rs992353(A;G) |
| Make rs992353(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 3 |
| Position | 156538672 |
| Gene | KCNAB1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs992353 |
| dbSNP (classic) | rs992353 |
| ClinGen | rs992353 |
| ebi | rs992353 |
| HLI | rs992353 |
| Exac | rs992353 |
| Gnomad | rs992353 |
| Varsome | rs992353 |
| LitVar | rs992353 |
| Map | rs992353 |
| PheGenI | rs992353 |
| Biobank | rs992353 |
| 1000 genomes | rs992353 |
| hgdp | rs992353 |
| ensembl | rs992353 |
| geneview | rs992353 |
| scholar | rs992353 |
| rs992353 | |
| pharmgkb | rs992353 |
| gwascentral | rs992353 |
| openSNP | rs992353 |
| 23andMe | rs992353 |
| SNPshot | rs992353 |
| SNPdbe | rs992353 |
| MSV3d | rs992353 |
| GWAS Ctlg | rs992353 |
| GMAF | 0.4399 |
| Max Magnitude | 0 |
[PMID 21333500] Association of intronic variants of the KCNAB1 gene with lateral temporal epilepsy
