rs121912665
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| Make rs121912665(C;T) |
| Make rs121912665(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 17 |
| Position | 7674965 |
| Gene | TP53 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs121912665 |
| dbSNP (classic) | rs121912665 |
| ClinGen | rs121912665 |
| ebi | rs121912665 |
| HLI | rs121912665 |
| Exac | rs121912665 |
| Gnomad | rs121912665 |
| Varsome | rs121912665 |
| LitVar | rs121912665 |
| Map | rs121912665 |
| PheGenI | rs121912665 |
| Biobank | rs121912665 |
| 1000 genomes | rs121912665 |
| hgdp | rs121912665 |
| ensembl | rs121912665 |
| geneview | rs121912665 |
| scholar | rs121912665 |
| rs121912665 | |
| pharmgkb | rs121912665 |
| gwascentral | rs121912665 |
| openSNP | rs121912665 |
| 23andMe | rs121912665 |
| SNPshot | rs121912665 |
| SNPdbe | rs121912665 |
| MSV3d | rs121912665 |
| GWAS Ctlg | rs121912665 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs121912665(T;T) |
| Alt | rs121912665(T;T) |
| Reference | Rs121912665(C;C) |
| Significance | Pathogenic |
| Disease | Familial colorectal cancer Hereditary cancer-predisposing syndrome Li-Fraumeni syndrome 1 |
| Variation | info |
| Gene | TP53 |
| CLNDBN | Familial colorectal cancer Hereditary cancer-predisposing syndrome Li-Fraumeni syndrome 1 |
| Reversed | 1 |
| HGVS | NC_000017.10:g.7578283G>A |
| CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
| CLNACC | RCV000013182.23, RCV000132058.3, RCV000144671.1, |
[PMID 31824279
] Advanced Invasive Extramammary Paget's Disease Concomitant with Cecal Cancer Possessing Rare Variant of TP53 Single Nucleotide Polymorphism.
