rs780442292
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 0 | common in clinvar |
| (A;C) | 7 | Li-Fraumeni Syndrome (predicted) |
| Make rs780442292(C;C) |
| Reference | GRCh38.p2 38.2/147 |
| Chromosome | 17 |
| Position | 7675211 |
| Gene | TP53 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs780442292 |
| dbSNP (classic) | rs780442292 |
| ClinGen | rs780442292 |
| ebi | rs780442292 |
| HLI | rs780442292 |
| Exac | rs780442292 |
| Gnomad | rs780442292 |
| Varsome | rs780442292 |
| LitVar | rs780442292 |
| Map | rs780442292 |
| PheGenI | rs780442292 |
| Biobank | rs780442292 |
| 1000 genomes | rs780442292 |
| hgdp | rs780442292 |
| ensembl | rs780442292 |
| geneview | rs780442292 |
| scholar | rs780442292 |
| rs780442292 | |
| pharmgkb | rs780442292 |
| gwascentral | rs780442292 |
| openSNP | rs780442292 |
| 23andMe | rs780442292 |
| SNPshot | rs780442292 |
| SNPdbe | rs780442292 |
| MSV3d | rs780442292 |
| GWAS Ctlg | rs780442292 |
| Max Magnitude | 7 |
| ClinVar | |
|---|---|
| Risk | rs780442292(C;C) |
| Alt | rs780442292(C;C) |
| Reference | Rs780442292(A;A) |
| Significance | Probable-Pathogenic |
| Disease | Hereditary cancer-predisposing syndrome |
| Variation | info |
| Gene | TP53 |
| CLNDBN | Hereditary cancer-predisposing syndrome |
| Reversed | 0 |
| HGVS | NC_000017.10:g.7578529A>C |
| CLNSRC | |
| CLNACC | RCV000214547.1, |
