rs3088440
| Orientation | plus |
| Stabilized | plus |
| Make rs3088440(A;A) |
| Make rs3088440(A;G) |
| Make rs3088440(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 9 |
| Position | 21968160 |
| Gene | CDKN2A, CDKN2A-AS1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs3088440 |
| dbSNP (classic) | rs3088440 |
| ClinGen | rs3088440 |
| ebi | rs3088440 |
| HLI | rs3088440 |
| Exac | rs3088440 |
| Gnomad | rs3088440 |
| Varsome | rs3088440 |
| LitVar | rs3088440 |
| Map | rs3088440 |
| PheGenI | rs3088440 |
| Biobank | rs3088440 |
| 1000 genomes | rs3088440 |
| hgdp | rs3088440 |
| ensembl | rs3088440 |
| geneview | rs3088440 |
| scholar | rs3088440 |
| rs3088440 | |
| pharmgkb | rs3088440 |
| gwascentral | rs3088440 |
| openSNP | rs3088440 |
| 23andMe | rs3088440 |
| SNPshot | rs3088440 |
| SNPdbe | rs3088440 |
| MSV3d | rs3088440 |
| GWAS Ctlg | rs3088440 |
| GMAF | 0.1483 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
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[PMID 19559344] Genetic variants on chromosome 9p21 and ischemic stroke in Chinese
[PMID 21061336] p14ARF genetic polymorphisms and susceptibility to second primary malignancy in patients with index squamous cell carcinoma of the head and neck
[PMID 21567202] Association analysis of p16 (CDKN2A) and RB1 polymorphisms with susceptibility to cervical cancer in Indian population
[PMID 12778444] [Polymorphism of two novel SNPs, which locate on chromosome 9p21-22, in Han Chinese of Hunan].
[PMID 17459456
] A common variant of the p16(INK4a) genetic region is associated with physical function in older people.
[PMID 17505013] Aurora-A and p16 polymorphisms contribute to an earlier age at diagnosis of pancreatic cancer in Caucasians.
[PMID 18174243] Association of single-nucleotide polymorphisms in the cell cycle genes with breast cancer in the British population.
[PMID 18454203] Differential allelic expression in the human genome: a robust approach to identify genetic and epigenetic cis-acting mechanisms regulating gene expression.
[PMID 18761660] Linkage and association study of late-onset Alzheimer disease families linked to 9p21.3.
[PMID 19224585] Genotype and haplotype analysis of cell cycle genes in sporadic colorectal cancer in the Czech Republic.
[PMID 19258477] Candidate gene analysis using imputed genotypes: cell cycle single-nucleotide polymorphisms and ovarian cancer risk.
[PMID 20386740] Chromosome 9p21 SNPs Associated with Multiple Disease Phenotypes Correlate with ANRIL Expression.
[PMID 20455025] Survey of familial glioma and role of germline p16INK4A/p14ARF and p53 mutation.
[PMID 21381012] p14ARF genetic polymorphisms and susceptibility to second primary malignancy in patients with index squamous cell carcinoma of the head and neck.
[PMID 23534750] Polymorphisms in TP53 (rs1042522), p16 (rs11515 and rs3088440) and NQO1 (rs1800566) Genes in Thai Cervical Cancer Patients with HPV 16 Infection
[PMID 24104554] Potentially functional variants of p14ARF are associated with HPV-positive oropharyngeal cancer patients and survival after definitive chemoradiotherapy
[PMID 23218882] Significance of MDM2 and P14 ARF polymorphisms in susceptibility to differentiated thyroid carcinoma.
[PMID 28445979] The impacts of single nucleotide polymorphisms in genes of cell cycle and NF-kB pathways on the efficacy and acute toxicities of radiotherapy in patients with nasopharyngeal carcinoma.
[PMID 31028217] Impact of MDM2, TP53 and P14ARF Polymorphisms on Endometrial Cancer Risk and Onset.
[PMID 32379408] Selected CDKN2A and MDM2 polymorphisms in oral cavity cancer.
