rs35117667
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| Make rs35117667(C;T) |
| Make rs35117667(T;T) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 17 |
| Position | 7676278 |
| Gene | TP53 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs35117667 |
| dbSNP (classic) | rs35117667 |
| ClinGen | rs35117667 |
| ebi | rs35117667 |
| HLI | rs35117667 |
| Exac | rs35117667 |
| Gnomad | rs35117667 |
| Varsome | rs35117667 |
| LitVar | rs35117667 |
| Map | rs35117667 |
| PheGenI | rs35117667 |
| Biobank | rs35117667 |
| 1000 genomes | rs35117667 |
| hgdp | rs35117667 |
| ensembl | rs35117667 |
| geneview | rs35117667 |
| scholar | rs35117667 |
| rs35117667 | |
| pharmgkb | rs35117667 |
| gwascentral | rs35117667 |
| openSNP | rs35117667 |
| 23andMe | rs35117667 |
| SNPshot | rs35117667 |
| SNPdbe | rs35117667 |
| MSV3d | rs35117667 |
| GWAS Ctlg | rs35117667 |
| GMAF | 0.00551 |
| Max Magnitude | 0 |
[PMID 24324286
] Investigation of genetic polymorphisms related to the outcome of radiotherapy for prostate cancer patients
| ClinVar | |
|---|---|
| Risk | rs35117667(T;T) |
| Alt | rs35117667(T;T) |
| Reference | Rs35117667(C;C) |
| Significance | Other |
| Disease | Li-Fraumeni syndrome |
| Variation | info |
| Gene | TP53 |
| CLNDBN | Li-Fraumeni syndrome |
| Reversed | 1 |
| HGVS | NC_000017.10:g.7579596G>A |
| CLNSRC | |
| CLNACC | RCV000206386.4, |
