rs10788160
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs10788160(A;A) |
| Make rs10788160(A;G) |
| Make rs10788160(G;G) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 10 |
| Position | 121274035 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs10788160 |
| dbSNP (classic) | rs10788160 |
| ClinGen | rs10788160 |
| ebi | rs10788160 |
| HLI | rs10788160 |
| Exac | rs10788160 |
| Gnomad | rs10788160 |
| Varsome | rs10788160 |
| LitVar | rs10788160 |
| Map | rs10788160 |
| PheGenI | rs10788160 |
| Biobank | rs10788160 |
| 1000 genomes | rs10788160 |
| hgdp | rs10788160 |
| ensembl | rs10788160 |
| geneview | rs10788160 |
| scholar | rs10788160 |
| rs10788160 | |
| pharmgkb | rs10788160 |
| gwascentral | rs10788160 |
| openSNP | rs10788160 |
| 23andMe | rs10788160 |
| SNPshot | rs10788160 |
| SNPdbe | rs10788160 |
| MSV3d | rs10788160 |
| GWAS Ctlg | rs10788160 |
| GMAF | 0.174 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 21160077 ]
|
| Trait | |
| Title | Genetic Correction of PSA Values Using Sequence Variants Associated with PSA Levels |
| Risk Allele | A |
| P-val | 5E-15 |
| Odds Ratio | 10.2000 [NR] % increase |
[PMID 23937305] Validation of association of genetic variants at 10q with prostate-specific antigen (PSA) levels in men at high risk for prostate cancer
[PMID 24345439] Prostate cancer risk alleles are associated with prostate cancer tumor volume and prostate size
[PMID 23246478] Personalized prostate specific antigen testing using genetic variants may reduce unnecessary prostate biopsies.
