rs3731217
| Orientation | minus |
| Stabilized | minus |
| Make rs3731217(G;G) |
| Make rs3731217(G;T) |
| Make rs3731217(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 9 |
| Position | 21984662 |
| Gene | CDKN2A |
| is a | snp |
| is | mentioned by |
| dbSNP | rs3731217 |
| dbSNP (classic) | rs3731217 |
| ClinGen | rs3731217 |
| ebi | rs3731217 |
| HLI | rs3731217 |
| Exac | rs3731217 |
| Gnomad | rs3731217 |
| Varsome | rs3731217 |
| LitVar | rs3731217 |
| Map | rs3731217 |
| PheGenI | rs3731217 |
| Biobank | rs3731217 |
| 1000 genomes | rs3731217 |
| hgdp | rs3731217 |
| ensembl | rs3731217 |
| geneview | rs3731217 |
| scholar | rs3731217 |
| rs3731217 | |
| pharmgkb | rs3731217 |
| gwascentral | rs3731217 |
| openSNP | rs3731217 |
| 23andMe | rs3731217 |
| SNPshot | rs3731217 |
| SNPdbe | rs3731217 |
| MSV3d | rs3731217 |
| GWAS Ctlg | rs3731217 |
| GMAF | 0.152 |
| Max Magnitude | 0 |
| ? | (G;G) (G;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 21061336] p14ARF genetic polymorphisms and susceptibility to second primary malignancy in patients with index squamous cell carcinoma of the head and neck
[PMID 20453839
] Variation in CDKN2A at 9p21.3 influences childhood acute lymphoblastic leukemia risk.
[PMID 20919861] Variation at 7p12.2 and 10q21.2 influences childhood acute lymphoblastic leukemia risk in the Thai population and may contribute to racial differences in leukemia incidence.
[PMID 21381012] p14ARF genetic polymorphisms and susceptibility to second primary malignancy in patients with index squamous cell carcinoma of the head and neck.
[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.
| GWAS snp | |
|---|---|
| PMID | [PMID 23996088] |
| Trait | Acute lymphoblastic leukemia (B-cell precursor) |
| Title | Variation at 10p12.2 and 10p14 influences risk of childhood B-cell acute lymphoblastic leukemia and phenotype. |
| Risk Allele | |
| P-val | 2E-8 |
| Odds Ratio | NR NR |
[PMID 26575185] Somatic Mutation Allelic Ratio Test Using ddPCR (SMART-ddPCR): An Accurate Method for Assessment of Preferential Allelic Imbalance in Tumor DNA
[PMID 27279837] Analysis of possible genetic risk factors contributing to development of childhood acute lymphoblastic leukaemia in the Latvian population.
[PMID 28768142] Contributions of IKZF1, DDC, CDKN2A, CEBPE, and LMO1 Gene Polymorphisms to Acute Lymphoblastic Leukemia in a Yemeni Population.
[PMID 31028217] Impact of MDM2, TP53 and P14ARF Polymorphisms on Endometrial Cancer Risk and Onset.
