rs10188577
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs10188577(C;C) |
| Make rs10188577(C;T) |
| Make rs10188577(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 2 |
| Position | 166059387 |
| Gene | SCN1A |
| is a | snp |
| is | mentioned by |
| dbSNP | rs10188577 |
| dbSNP (classic) | rs10188577 |
| ClinGen | rs10188577 |
| ebi | rs10188577 |
| HLI | rs10188577 |
| Exac | rs10188577 |
| Gnomad | rs10188577 |
| Varsome | rs10188577 |
| LitVar | rs10188577 |
| Map | rs10188577 |
| PheGenI | rs10188577 |
| Biobank | rs10188577 |
| 1000 genomes | rs10188577 |
| hgdp | rs10188577 |
| ensembl | rs10188577 |
| geneview | rs10188577 |
| scholar | rs10188577 |
| rs10188577 | |
| pharmgkb | rs10188577 |
| gwascentral | rs10188577 |
| openSNP | rs10188577 |
| 23andMe | rs10188577 |
| SNPshot | rs10188577 |
| SNPdbe | rs10188577 |
| MSV3d | rs10188577 |
| GWAS Ctlg | rs10188577 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 24337656] Case-control association study of polymorphisms in the voltage-gated sodium channel genes SCN1A, SCN2A, SCN3A, SCN1B, and SCN2B and epilepsy
[PMID 24342961] SCN1A variations and response to multiple antiepileptic drugs
[PMID 30693367] SCN1A and SCN2A polymorphisms are associated with response to valproic acid in Chinese epilepsy patients.
