rs121909282
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (T;T) | 0 | common in clinvar |
| Make rs121909282(G;G) |
| Make rs121909282(G;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 3 |
| Position | 8745647 |
| Gene | CAV3, SSUH2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs121909282 |
| dbSNP (classic) | rs121909282 |
| ClinGen | rs121909282 |
| ebi | rs121909282 |
| HLI | rs121909282 |
| Exac | rs121909282 |
| Gnomad | rs121909282 |
| Varsome | rs121909282 |
| LitVar | rs121909282 |
| Map | rs121909282 |
| PheGenI | rs121909282 |
| Biobank | rs121909282 |
| 1000 genomes | rs121909282 |
| hgdp | rs121909282 |
| ensembl | rs121909282 |
| geneview | rs121909282 |
| scholar | rs121909282 |
| rs121909282 | |
| pharmgkb | rs121909282 |
| gwascentral | rs121909282 |
| openSNP | rs121909282 |
| 23andMe | rs121909282 |
| SNPshot | rs121909282 |
| SNPdbe | rs121909282 |
| MSV3d | rs121909282 |
| GWAS Ctlg | rs121909282 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs121909282(G;G) |
| Alt | rs121909282(G;G) |
| Reference | Rs121909282(T;T) |
| Significance | Pathogenic |
| Disease | Long QT syndrome 9 not provided |
| Variation | info |
| Gene | SSUH2 CAV3 |
| CLNDBN | Long QT syndrome 9 not provided |
| Reversed | 0 |
| HGVS | NC_000003.11:g.8787333T>G |
| CLNSRC | Leiden Muscular Dystrophy pages (CAV3) OMIM Allelic Variant UniProtKB (protein) |
| CLNACC | RCV000008794.2, RCV000024434.1, |
[PMID 17275750
] Novel mechanism for sudden infant death syndrome: persistent late sodium current secondary to mutations in caveolin-3.
