rs17883323
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| Make rs17883323(A;A) |
| Make rs17883323(A;C) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 17 |
| Position | 7676301 |
| Gene | TP53 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs17883323 |
| dbSNP (classic) | rs17883323 |
| ClinGen | rs17883323 |
| ebi | rs17883323 |
| HLI | rs17883323 |
| Exac | rs17883323 |
| Gnomad | rs17883323 |
| Varsome | rs17883323 |
| LitVar | rs17883323 |
| Map | rs17883323 |
| PheGenI | rs17883323 |
| Biobank | rs17883323 |
| 1000 genomes | rs17883323 |
| hgdp | rs17883323 |
| ensembl | rs17883323 |
| geneview | rs17883323 |
| scholar | rs17883323 |
| rs17883323 | |
| pharmgkb | rs17883323 |
| gwascentral | rs17883323 |
| openSNP | rs17883323 |
| 23andMe | rs17883323 |
| SNPshot | rs17883323 |
| SNPdbe | rs17883323 |
| MSV3d | rs17883323 |
| GWAS Ctlg | rs17883323 |
| GMAF | 0.07346 |
| Max Magnitude | 0 |
[PMID 24324286
] Investigation of genetic polymorphisms related to the outcome of radiotherapy for prostate cancer patients
[PMID 18849522] Nested Patch PCR enables highly multiplexed mutation discovery in candidate genes.
[PMID 19426493] A case-control study on the combined effects of p53 and p73 polymorphisms on head and neck cancer risk in an Italian population.
| ClinVar | |
|---|---|
| Risk | rs17883323(A;A) |
| Alt | rs17883323(A;A) |
| Reference | Rs17883323(C;C) |
| Significance | Non-pathogenic |
| Disease | not specified |
| Variation | info |
| Gene | TP53 |
| CLNDBN | not specified |
| Reversed | 1 |
| HGVS | NC_000017.10:g.7579619G>T |
| CLNSRC | |
| CLNACC | RCV000242439.1, |
