rs2082366
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs2082366(C;C) |
| Make rs2082366(C;G) |
| Make rs2082366(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 2 |
| Position | 165402907 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2082366 |
| dbSNP (classic) | rs2082366 |
| ClinGen | rs2082366 |
| ebi | rs2082366 |
| HLI | rs2082366 |
| Exac | rs2082366 |
| Gnomad | rs2082366 |
| Varsome | rs2082366 |
| LitVar | rs2082366 |
| Map | rs2082366 |
| PheGenI | rs2082366 |
| Biobank | rs2082366 |
| 1000 genomes | rs2082366 |
| hgdp | rs2082366 |
| ensembl | rs2082366 |
| geneview | rs2082366 |
| scholar | rs2082366 |
| rs2082366 | |
| pharmgkb | rs2082366 |
| gwascentral | rs2082366 |
| openSNP | rs2082366 |
| 23andMe | rs2082366 |
| SNPshot | rs2082366 |
| SNPdbe | rs2082366 |
| MSV3d | rs2082366 |
| GWAS Ctlg | rs2082366 |
| Max Magnitude | 0 |
| ? | (C;C) (C;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 24337656] Case-control association study of polymorphisms in the voltage-gated sodium channel genes SCN1A, SCN2A, SCN3A, SCN1B, and SCN2B and epilepsy
