rs199476337
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (T;T) | 0 | common in clinvar |
| Make rs199476337(C;C) |
| Make rs199476337(C;T) |
| Reference | GRCh38.p7 38.3/149 |
| Chromosome | 3 |
| Position | 8745712 |
| Gene | CAV3, SSUH2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs199476337 |
| dbSNP (classic) | rs199476337 |
| ClinGen | rs199476337 |
| ebi | rs199476337 |
| HLI | rs199476337 |
| Exac | rs199476337 |
| Gnomad | rs199476337 |
| Varsome | rs199476337 |
| LitVar | rs199476337 |
| Map | rs199476337 |
| PheGenI | rs199476337 |
| Biobank | rs199476337 |
| 1000 genomes | rs199476337 |
| hgdp | rs199476337 |
| ensembl | rs199476337 |
| geneview | rs199476337 |
| scholar | rs199476337 |
| rs199476337 | |
| pharmgkb | rs199476337 |
| gwascentral | rs199476337 |
| openSNP | rs199476337 |
| 23andMe | rs199476337 |
| SNPshot | rs199476337 |
| SNPdbe | rs199476337 |
| MSV3d | rs199476337 |
| GWAS Ctlg | rs199476337 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs199476337(C;C) |
| Alt | rs199476337(C;C) |
| Reference | Rs199476337(T;T) |
| Significance | Untested |
| Disease | not provided |
| Variation | info |
| Gene | SSUH2 CAV3 |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000003.11:g.8787398T>C |
| CLNSRC | Leiden Muscular Dystrophy pages (CAV3) |
| CLNACC | RCV000024420.1, |
