rs17887200
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 0 | common in complete genomics |
| Make rs17887200(A;G) |
| Make rs17887200(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 17 |
| Position | 7667753 |
| Gene | TP53 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs17887200 |
| dbSNP (classic) | rs17887200 |
| ClinGen | rs17887200 |
| ebi | rs17887200 |
| HLI | rs17887200 |
| Exac | rs17887200 |
| Gnomad | rs17887200 |
| Varsome | rs17887200 |
| LitVar | rs17887200 |
| Map | rs17887200 |
| PheGenI | rs17887200 |
| Biobank | rs17887200 |
| 1000 genomes | rs17887200 |
| hgdp | rs17887200 |
| ensembl | rs17887200 |
| geneview | rs17887200 |
| scholar | rs17887200 |
| rs17887200 | |
| pharmgkb | rs17887200 |
| gwascentral | rs17887200 |
| openSNP | rs17887200 |
| 23andMe | rs17887200 |
| SNPshot | rs17887200 |
| SNPdbe | rs17887200 |
| MSV3d | rs17887200 |
| GWAS Ctlg | rs17887200 |
| GMAF | 0.1511 |
| Max Magnitude | 0 |
[PMID 17683073] rs17887200 and rs12951053 associated with ER negative breast cancer tumors (1.48 (1.11-1.93) p-trend = 0.01 and 1.29 (1.06-1.58) p-trend = 0.009, respectively)
[PMID 17428325
] Common variants in the ATM, BRCA1, BRCA2, CHEK2 and TP53 cancer susceptibility genes are unlikely to increase breast cancer risk.
[PMID 19423538] Common genetic variation in TP53 and risk of human papillomavirus persistence and progression to CIN3/cancer revisited.
