rs17878362
Orientation | plus |
Stabilized | minus |
Make rs17878362(-;-) |
Make rs17878362(-;ACCTGGAGGGCTGGGG) |
Make rs17878362(ACCTGGAGGGCTGGGG;ACCTGGAGGGCTGGGG) |
Reference | GRCh38 38.1/142 |
Chromosome | 17 |
Position | 7676326 |
Gene | TP53 |
is a | snp |
is | mentioned by |
dbSNP | rs17878362 |
dbSNP (classic) | rs17878362 |
ClinGen | rs17878362 |
ebi | rs17878362 |
HLI | rs17878362 |
Exac | rs17878362 |
Gnomad | rs17878362 |
Varsome | rs17878362 |
LitVar | rs17878362 |
Map | rs17878362 |
PheGenI | rs17878362 |
Biobank | rs17878362 |
1000 genomes | rs17878362 |
hgdp | rs17878362 |
ensembl | rs17878362 |
geneview | rs17878362 |
scholar | rs17878362 |
rs17878362 | |
pharmgkb | rs17878362 |
gwascentral | rs17878362 |
openSNP | rs17878362 |
23andMe | rs17878362 |
SNPshot | rs17878362 |
SNPdbe | rs17878362 |
MSV3d | rs17878362 |
GWAS Ctlg | rs17878362 |
Status | Deleted |
Max Magnitude | 0 |
*[PMID 19193430] rs2279744, rs1042522, rs17878362 and rs1625895 associated with high grade endometrial cancer
[PMID 19505915] Association of Genetic Polymorphisms, mRNA Expression of p53 and p21 with Chronic Benzene Poisoning in a Chinese Occupational Population
[PMID 20110284] Genotype and haplotype analysis of TP53 gene and the risk of pancreatic cancer: an association study in the Czech Republic
[PMID 21473292] Association of TP53 intron 3, 16 bp duplication polymorphism with esophageal and gastric cancer susceptibility in Kashmir Valley
[PMID 21838531] Crosstalk between the FGFR2 and TP53 genes in breast cancer: data from an association study and epistatic interaction analysis
[PMID 22669776] Discovery of TP53 splice variants in two novel papillary urothelial cancer cell lines
[PMID 17624591] Genetic variation of TP53, polycyclic aromatic hydrocarbon-related exposures, and breast cancer risk among women on Long Island, New York.
[PMID 18332046] A distinct ERCC1 haplotype is associated with mRNA expression levels in prostate cancer patients.
[PMID 18798306] Construction of a high resolution linkage disequilibrium map to evaluate common genetic variation in TP53 and neural tube defect risk in an Irish population.
[PMID 19224585] Genotype and haplotype analysis of cell cycle genes in sporadic colorectal cancer in the Czech Republic.
[PMID 19542078] TP53 PIN3 and MDM2 SNP309 polymorphisms as genetic modifiers in the Li-Fraumeni syndrome: impact on age at first diagnosis.
[PMID 19784392] Primary open angle glaucoma in a Caucasian population is associated with the p53 codon 72 polymorphism.
[PMID 21810023] Coordination of TP53 abnormalities in breast cancer: data from analysis of TP53 polymorphisms, loss of heterozygosity, methylation, and mutations.
[PMID 23412385] A meta-analysis of cancer risk associated with the TP53 intron 3 duplication polymorphism (rs17878362): geographic and tumor-specific effects
[PMID 23360829] Association between polymorphisms in the genes for tumor suppressor protein p53 and its regulator NAD(P)H: quinone oxidoreductase 1 (NQO1) and schizophrenia in a Syrian study cohort
[PMID 24324286] Investigation of genetic polymorphisms related to the outcome of radiotherapy for prostate cancer patients
[PMID 26003292] Effect of TP53 16-bp and β-TrCP 9-bp INS/DEL polymorphisms in relation to risk of breast cancer
[PMID 26586794] The presence of the intron 3 16bp duplication polymorphism of p53 (rs17878362) in breast cancer is associated with a low Δ40p53:p53 ratio and better outcome
[PMID 31387111] Haplotype and linkage disequilibrium of TP53-WRAP53 locus in Iranian-Azeri women with breast cancer.