rs879253730
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs879253730(C;G) |
| Make rs879253730(G;G) |
| Reference | GRCh38.p2 38.2/147 |
| Chromosome | 11 |
| Position | 123642468 |
| Gene | SCN3B |
| is a | snp |
| is | mentioned by |
| dbSNP | rs879253730 |
| dbSNP (classic) | rs879253730 |
| ClinGen | rs879253730 |
| ebi | rs879253730 |
| HLI | rs879253730 |
| Exac | rs879253730 |
| Gnomad | rs879253730 |
| Varsome | rs879253730 |
| LitVar | rs879253730 |
| Map | rs879253730 |
| PheGenI | rs879253730 |
| Biobank | rs879253730 |
| 1000 genomes | rs879253730 |
| hgdp | rs879253730 |
| ensembl | rs879253730 |
| geneview | rs879253730 |
| scholar | rs879253730 |
| rs879253730 | |
| pharmgkb | rs879253730 |
| gwascentral | rs879253730 |
| openSNP | rs879253730 |
| 23andMe | rs879253730 |
| SNPshot | rs879253730 |
| SNPdbe | rs879253730 |
| MSV3d | rs879253730 |
| GWAS Ctlg | rs879253730 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs879253730(G;G) |
| Alt | rs879253730(G;G) |
| Reference | Rs879253730(C;C) |
| Significance | Pathogenic |
| Disease | Arrhythmia |
| Variation | info |
| Gene | SCN3B |
| CLNDBN | Arrhythmia |
| Reversed | 1 |
| HGVS | NC_000011.9:g.123513176G>C |
| CLNSRC | |
| CLNACC | RCV000234971.1, |
