rs7127900
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs7127900(A;A) |
| Make rs7127900(A;G) |
| Make rs7127900(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 11 |
| Position | 2212344 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs7127900 |
| dbSNP (classic) | rs7127900 |
| ClinGen | rs7127900 |
| ebi | rs7127900 |
| HLI | rs7127900 |
| Exac | rs7127900 |
| Gnomad | rs7127900 |
| Varsome | rs7127900 |
| LitVar | rs7127900 |
| Map | rs7127900 |
| PheGenI | rs7127900 |
| Biobank | rs7127900 |
| 1000 genomes | rs7127900 |
| hgdp | rs7127900 |
| ensembl | rs7127900 |
| geneview | rs7127900 |
| scholar | rs7127900 |
| rs7127900 | |
| pharmgkb | rs7127900 |
| gwascentral | rs7127900 |
| openSNP | rs7127900 |
| 23andMe | rs7127900 |
| SNPshot | rs7127900 |
| SNPdbe | rs7127900 |
| MSV3d | rs7127900 |
| GWAS Ctlg | rs7127900 |
| GMAF | 0.2502 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 19767753 ]
|
| Trait | Prostate cancer |
| Title | Identification of seven new prostate cancer susceptibility loci through a genome-wide association study |
| Risk Allele | A |
| P-val | 3E-33 |
| Odds Ratio | 1.22 [1.17-1.27] |
[PMID 22253814] A multi-cohort study of polymorphisms in the GH/IGF axis and physical capability: the HALCyon programme
[PMID 22219177] A Genome-Wide Search for Loci Interacting with Known Prostate Cancer Risk-Associated Genetic Variants.
[PMID 21390317] Characterizing associations and SNP-environment interactions for GWAS-identified prostate cancer risk markers--results from BPC3.
[PMID 24411283] Prostate Cancer (PCa) Risk Variants and Risk of Fatal PCa in the National Cancer Institute Breast and Prostate Cancer Cohort Consortium
| GWAS snp | |
|---|---|
| PMID | [PMID 24740154]
|
| Trait | Prostate cancer (early onset) |
| Title | Genome-wide association scan for variants associated with early-onset prostate cancer. |
| Risk Allele | A |
| P-val | 1E-7 |
| Odds Ratio | 1.40 [NR] |
