rs2735839
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 1.8 | in prostrate cancer patients, this is statistically associated with a somewhat more aggressive cancer |
| (A;G) | 1.6 | in prostrate cancer patients, this is statistically associated with a somewhat more aggressive cancer |
| (G;G) | 0 |
| Reference | GRCh38 38.1/141 |
| Chromosome | 19 |
| Position | 50861367 |
| Gene | KLK3 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2735839 |
| dbSNP (classic) | rs2735839 |
| ClinGen | rs2735839 |
| ebi | rs2735839 |
| HLI | rs2735839 |
| Exac | rs2735839 |
| Gnomad | rs2735839 |
| Varsome | rs2735839 |
| LitVar | rs2735839 |
| Map | rs2735839 |
| PheGenI | rs2735839 |
| Biobank | rs2735839 |
| 1000 genomes | rs2735839 |
| hgdp | rs2735839 |
| ensembl | rs2735839 |
| geneview | rs2735839 |
| scholar | rs2735839 |
| rs2735839 | |
| pharmgkb | rs2735839 |
| gwascentral | rs2735839 |
| openSNP | rs2735839 |
| 23andMe | rs2735839 |
| SNPshot | rs2735839 |
| SNPdbe | rs2735839 |
| MSV3d | rs2735839 |
| GWAS Ctlg | rs2735839 |
| GMAF | 0.2916 |
| Max Magnitude | 1.8 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 25274378
] A study of ~1,800 Caucasian prostate cancer patients concludes that the rs2735839(A) allele is associated with aggressive prostate cancer in general, and more specifically, in Gleason score 7 patients, it is more often associated with being GS 4 + 3 rather than GS 3 + 4 (odd ratio 1.85, CI: 1.31-2.61).
cancer-genetics these snps influence genetic risk for prostate cancer
- the haplotype rs6983267 rs1016343 rs4242384
- rs7501939
- rs1859962
- rs2660753
- rs9364554
- rs6465657
- rs10993994
- rs7931342
- rs2735839
- rs5945619
- rs10993994
[PMID 19366831
] Genotyping 13 SNPs (including this one) in 1,308 Caucasian prostate cancer patients led to the conclusion that while none of the SNP associations were as significant as having a first-degree family history of the disease, they did replicate. And in fact, for rs2735839, the risk estimate varied by family history.
| GWAS | |
|---|---|
| SNP | rs2735839 |
| PubMedID | [PMID 18264097] |
| Condition | Prostate cancer |
| Gene | KLK3 |
| Risk Allele | G |
| pValue | 2.00E-018 |
| OR | 1.2 |
| 95% CI | 1.10-1.33 |
[PMID 19336566
] Replication of the 10q11 and Xp11 Prostate Cancer Risk Variants: Results from a Utah Pedigree-Based Study.
[PMID 19902474] Replication of prostate cancer risk loci on 8q24, 11q13, 17q12, 19q33, and Xp11 in African Americans
[PMID 20460480
] Susceptibility loci associated with prostate cancer progression and mortality
[PMID 21465221
] Identification of a novel prostate cancer susceptibility variant in the KLK3 gene transcript
[PMID 21390317
] Characterizing associations and SNP-environment interactions for GWAS-identified prostate cancer risk markers--results from BPC3
[PMID 22549899
] Genetic polymorphism and prostate cancer aggressiveness: A case-only study of 1,536 GWAS and candidate SNPs in African-Americans and European-Americans
[PMID 18708398
] Multiple novel prostate cancer predisposition loci confirmed by an international study: the PRACTICAL Consortium.
[PMID 18794092
] Association of prostate cancer risk variants with clinicopathologic characteristics of the disease.
[PMID 18974127
] Association study of prostate cancer susceptibility variants with risks of invasive ovarian, breast, and colorectal cancer.
[PMID 19104501
] Prostate cancer genomics: towards a new understanding.
[PMID 19153072
] Fine mapping association study and functional analysis implicate a SNP in MSMB at 10q11 as a causal variant for prostate cancer risk.
[PMID 19318432
] Generalizability of associations from prostate cancer genome-wide association studies in multiple populations.
[PMID 19318570
] A novel prostate cancer susceptibility locus at 19q13.
[PMID 19434657
] Individual and cumulative effect of prostate cancer risk-associated variants on clinicopathologic variables in 5,895 prostate cancer patients.
[PMID 19505914
] Two independent prostate cancer risk-associated Loci at 11q13.
[PMID 19549807
] Prostate cancer risk associated loci in African Americans.
[PMID 19639606
] Correcting "winner's curse" in odds ratios from genomewide association findings for major complex human diseases.
[PMID 19823874
] A comprehensive resequence analysis of the KLK15-KLK3-KLK2 locus on chromosome 19q13.33.
[PMID 20039378
] Estimation of genotype relative risks from pedigree data by retrospective likelihoods.
[PMID 20369022
] Candidate causal regulatory effects by integration of expression QTLs with complex trait genetic associations.
[PMID 20690139] Meta-analysis of genome-wide and replication association studies on prostate cancer.
[PMID 21318478
] Fine mapping the KLK3 locus on chromosome 19q13.33 associated with prostate cancer susceptibility and PSA levels.
[PMID 21367958
] Association of prostate cancer risk Loci with disease aggressiveness and prostate cancer-specific mortality.
[PMID 21538423
] Early onset prostate cancer has a significant genetic component.
| GWAS snp | |
|---|---|
| PMID | [PMID 23269536] |
| Trait | Prostate-specific antigen levels |
| Title | Genome-wide association study identified novel genetic variant on SLC45A3 gene associated with serum levels prostate-specific antigen (PSA) in a Chinese population. |
| Risk Allele | G |
| P-val | 6E-37 |
| Odds Ratio | .19 [NR] % higher levels |
[PMID 24411283
] Prostate Cancer (PCa) Risk Variants and Risk of Fatal PCa in the National Cancer Institute Breast and Prostate Cancer Cohort Consortium
[PMID 22901566] Effectiveness of the combined evaluation of KLK3 genetics and free-to-total prostate specific antigen ratio for prostate cancer diagnosis.
[PMID 23543094
] Testing for associations between loci and environmental gradients using latent factor mixed models.
[PMID 25715684
] Associations of prostate cancer risk variants with disease aggressiveness: results of the NCI-SPORE Genetics Working Group analysis of 18,343 cases
[PMID 32295536
] Association study between common variations in some candidate genes and prostate adenocarcinoma predisposition through multi-stage approach in Iranian population.
