rs10896449
| Orientation | plus |
| Stabilized | plus |
| Make rs10896449(A;A) |
| Make rs10896449(A;G) |
| Make rs10896449(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 11 |
| Position | 69227200 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs10896449 |
| dbSNP (classic) | rs10896449 |
| ClinGen | rs10896449 |
| ebi | rs10896449 |
| HLI | rs10896449 |
| Exac | rs10896449 |
| Gnomad | rs10896449 |
| Varsome | rs10896449 |
| LitVar | rs10896449 |
| Map | rs10896449 |
| PheGenI | rs10896449 |
| Biobank | rs10896449 |
| 1000 genomes | rs10896449 |
| hgdp | rs10896449 |
| ensembl | rs10896449 |
| geneview | rs10896449 |
| scholar | rs10896449 |
| rs10896449 | |
| pharmgkb | rs10896449 |
| gwascentral | rs10896449 |
| openSNP | rs10896449 |
| 23andMe | rs10896449 |
| SNPshot | rs10896449 |
| SNPdbe | rs10896449 |
| MSV3d | rs10896449 |
| GWAS Ctlg | rs10896449 |
| GMAF | 0.4063 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
nature identifies rs10486567 rs10993994 rs10896449 in prostate cancer
| GWAS | |
|---|---|
| SNP | rs10896449 |
| PubMedID | [PMID 18264096] |
| Condition | Prostate cancer (aggressive) |
| Gene | Intergenic |
| Risk Allele | G |
| pValue | 2.00E-009 |
| OR | 1.1 |
| 95% CI | 0.98-1.23 |
[PMID 19505914
] Two independent prostate cancer risk-associated Loci at 11q13
[PMID 19902474] Replication of prostate cancer risk loci on 8q24, 11q13, 17q12, 19q33, and Xp11 in African Americans
[PMID 21531787] Fine mapping of a region of chromosome 11q13 reveals multiple independent loci associated with risk of prostate cancer
[PMID 22459122] Interactions Between Genome-wide Significant Genetic Variants and Circulating Concentrations of Insulin-like Growth Factor 1, Sex Hormones, and Binding Proteins in Relation to Prostate Cancer Risk in the National Cancer Institute Breast and Prostate Cancer Cohort Consortium
[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 19366831] Analysis of recently identified prostate cancer susceptibility loci in a population-based study: associations with family history and clinical features.
[PMID 19434657] Individual and cumulative effect of prostate cancer risk-associated variants on clinicopathologic variables in 5,895 prostate cancer patients.
[PMID 19549807] Prostate cancer risk associated loci in African Americans.
[PMID 19567509] Genetic variants and prostate cancer risk: candidate replication and exploration of viral restriction genes.
[PMID 20039378] Estimation of genotype relative risks from pedigree data by retrospective likelihoods.
[PMID 20569440] Alterations in LMTK2, MSMB and HNF1B gene expression are associated with the development of prostate cancer.
[PMID 20690139] Meta-analysis of genome-wide and replication association studies on prostate cancer.
[PMID 21390317] Characterizing associations and SNP-environment interactions for GWAS-identified prostate cancer risk markers--results from BPC3.
[PMID 21520160] Prostate cancer risk variants are not associated with disease progression.
[PMID 22468268] Comprehensive resequence analysis of a 123-kb region of chromosome 11q13 associated with prostate cancer.
[PMID 23405784] [Susceptibility to prostate cancer in Han Chinese: single nucleotide polymorphism analysis of 1 667 cases]
[PMID 23573233] Characterization of SNPs Associated with Prostate Cancer in Men of Ashkenazic Descent from the Set of GWAS Identified SNPs: Impact of Cancer Family History and Cumulative SNP Risk Prediction
