rs5744857
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs5744857(A;A) |
| Make rs5744857(A;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 12 |
| Position | 132659414 |
| Gene | POLE |
| is a | snp |
| is | mentioned by |
| dbSNP | rs5744857 |
| dbSNP (classic) | rs5744857 |
| ClinGen | rs5744857 |
| ebi | rs5744857 |
| HLI | rs5744857 |
| Exac | rs5744857 |
| Gnomad | rs5744857 |
| Varsome | rs5744857 |
| LitVar | rs5744857 |
| Map | rs5744857 |
| PheGenI | rs5744857 |
| Biobank | rs5744857 |
| 1000 genomes | rs5744857 |
| hgdp | rs5744857 |
| ensembl | rs5744857 |
| geneview | rs5744857 |
| scholar | rs5744857 |
| rs5744857 | |
| pharmgkb | rs5744857 |
| gwascentral | rs5744857 |
| openSNP | rs5744857 |
| 23andMe | rs5744857 |
| SNPshot | rs5744857 |
| SNPdbe | rs5744857 |
| MSV3d | rs5744857 |
| GWAS Ctlg | rs5744857 |
| GMAF | 0.416 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 20503108] VARS2 V552V variant as prognostic marker in patients with early breast cancer
| ClinVar | |
|---|---|
| Risk | rs5744857(A;A) |
| Alt | rs5744857(A;A) |
| Reference | Rs5744857(G;G) |
| Significance | Non-pathogenic |
| Disease | not specified Hereditary cancer-predisposing syndrome |
| Variation | info |
| Gene | POLE |
| CLNDBN | not specified Hereditary cancer-predisposing syndrome |
| Reversed | 1 |
| HGVS | NC_000012.11:g.133236000C>T |
| CLNSRC | |
| CLNACC | RCV000421896.1, RCV000492265.1, |
