rs5945619
| Orientation | plus |
| Stabilized | plus |
| Make rs5945619(C;C) |
| Make rs5945619(C;T) |
| Make rs5945619(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | X |
| Position | 51498820 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs5945619 |
| dbSNP (classic) | rs5945619 |
| ClinGen | rs5945619 |
| ebi | rs5945619 |
| HLI | rs5945619 |
| Exac | rs5945619 |
| Gnomad | rs5945619 |
| Varsome | rs5945619 |
| LitVar | rs5945619 |
| Map | rs5945619 |
| PheGenI | rs5945619 |
| Biobank | rs5945619 |
| 1000 genomes | rs5945619 |
| hgdp | rs5945619 |
| ensembl | rs5945619 |
| geneview | rs5945619 |
| scholar | rs5945619 |
| rs5945619 | |
| pharmgkb | rs5945619 |
| gwascentral | rs5945619 |
| openSNP | rs5945619 |
| 23andMe | rs5945619 |
| SNPshot | rs5945619 |
| SNPdbe | rs5945619 |
| MSV3d | rs5945619 |
| GWAS Ctlg | rs5945619 |
| GMAF | 0.2618 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
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 19336566
] Replication of the 10q11 and Xp11 Prostate Cancer Risk Variants: Results from a Utah Pedigree-Based Study.
[PMID 19366831
] Analysis of Recently Identified Prostate Cancer Susceptibility Loci in a Population-based Study: Associations with Family History and Clinical Features
| GWAS snp | |
|---|---|
| PMID | [PMID 18264097] |
| Trait | Prostate cancer |
| Title | Multiple newly identified loci associated with prostate cancer susceptibility |
| Risk Allele | C |
| P-val | 2.0000000000000001E-9 |
| Odds Ratio | 1.19 [1.07-1.31] |
[PMID 19549809
] Fine-Mapping and Family-Based Association Analyses of Prostate Cancer Risk Variants at Xp11
[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 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 19639606
] Correcting "winner's curse" in odds ratios from genomewide association findings for major complex human diseases.
[PMID 20039378
] Estimation of genotype relative risks from pedigree data by retrospective likelihoods.
[PMID 20690139] Meta-analysis of genome-wide and replication association studies on prostate cancer.
[PMID 21071540
] Validation of genome-wide prostate cancer associations in men of African descent.
[PMID 21390317
] Characterizing associations and SNP-environment interactions for GWAS-identified prostate cancer risk markers--results from BPC3.
[PMID 21538423
] Early onset prostate cancer has a significant genetic component.
- Is a snp
- In dbSNP
- SNPs on chromosome X
- Has genotype
- Has population
- Uses omim
- On chip 23andMe v1
- On chip 23andMe v2
- On chip 23andMe v3
- On chip 23andMe v4
- On chip Affy GenomeWide 6
- On chip Ancestry v2
- On chip FTDNA2
- On chip FTDNA
- On chip HumanOmni1Quad
- On chip Illumina Human 1M
- On chip 23andMe v5
- On chip Ancestry v2c
- On chip Ancestry v2d
