rs796053000
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs796053000(A;A) |
| Make rs796053000(A;G) |
| Reference | GRCh38.p2 38.2/146 |
| Chromosome | 2 |
| Position | 166012164 |
| Gene | LOC102724058, SCN1A |
| is a | snp |
| is | mentioned by |
| dbSNP | rs796053000 |
| dbSNP (classic) | rs796053000 |
| ClinGen | rs796053000 |
| ebi | rs796053000 |
| HLI | rs796053000 |
| Exac | rs796053000 |
| Gnomad | rs796053000 |
| Varsome | rs796053000 |
| LitVar | rs796053000 |
| Map | rs796053000 |
| PheGenI | rs796053000 |
| Biobank | rs796053000 |
| 1000 genomes | rs796053000 |
| hgdp | rs796053000 |
| ensembl | rs796053000 |
| geneview | rs796053000 |
| scholar | rs796053000 |
| rs796053000 | |
| pharmgkb | rs796053000 |
| gwascentral | rs796053000 |
| openSNP | rs796053000 |
| 23andMe | rs796053000 |
| SNPshot | rs796053000 |
| SNPdbe | rs796053000 |
| MSV3d | rs796053000 |
| GWAS Ctlg | rs796053000 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs796053000(A;A) |
| Alt | rs796053000(A;A) |
| Reference | Rs796053000(G;G) |
| Significance | Probable-Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | LOC102724058 SCN1A |
| CLNDBN | not provided |
| Reversed | 1 |
| HGVS | NC_000002.11:g.166868674C>T |
| CLNSRC | |
| CLNACC | RCV000188931.1, |
