rs570278423
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| Make rs570278423(C;T) |
| Make rs570278423(T;T) |
| Reference | GRCh38.p2 38.2/146 |
| Chromosome | 1 |
| Position | 17033077 |
| Gene | SDHB |
| is a | snp |
| is | mentioned by |
| dbSNP | rs570278423 |
| dbSNP (classic) | rs570278423 |
| ClinGen | rs570278423 |
| ebi | rs570278423 |
| HLI | rs570278423 |
| Exac | rs570278423 |
| Gnomad | rs570278423 |
| Varsome | rs570278423 |
| LitVar | rs570278423 |
| Map | rs570278423 |
| PheGenI | rs570278423 |
| Biobank | rs570278423 |
| 1000 genomes | rs570278423 |
| hgdp | rs570278423 |
| ensembl | rs570278423 |
| geneview | rs570278423 |
| scholar | rs570278423 |
| rs570278423 | |
| pharmgkb | rs570278423 |
| gwascentral | rs570278423 |
| openSNP | rs570278423 |
| 23andMe | rs570278423 |
| SNPshot | rs570278423 |
| SNPdbe | rs570278423 |
| MSV3d | rs570278423 |
| GWAS Ctlg | rs570278423 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs570278423(T;T) |
| Alt | rs570278423(T;T) |
| Reference | Rs570278423(C;C) |
| Significance | Probable-Pathogenic |
| Disease | Hereditary cancer-predisposing syndrome |
| Variation | info |
| Gene | SDHB |
| CLNDBN | Hereditary cancer-predisposing syndrome |
| Reversed | 0 |
| HGVS | NC_000001.10:g.17359572C>T |
| CLNSRC | |
| CLNACC | RCV000492424.1, |
