rs3087425
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| Make rs3087425(C;T) |
| Make rs3087425(T;T) |
| Reference | GRCh38.p2 38.2/146 |
| Chromosome | 8 |
| Position | 31120294 |
| Gene | WRN |
| is a | snp |
| is | mentioned by |
| dbSNP | rs3087425 |
| dbSNP (classic) | rs3087425 |
| ClinGen | rs3087425 |
| ebi | rs3087425 |
| HLI | rs3087425 |
| Exac | rs3087425 |
| Gnomad | rs3087425 |
| Varsome | rs3087425 |
| LitVar | rs3087425 |
| Map | rs3087425 |
| PheGenI | rs3087425 |
| Biobank | rs3087425 |
| 1000 genomes | rs3087425 |
| hgdp | rs3087425 |
| ensembl | rs3087425 |
| geneview | rs3087425 |
| scholar | rs3087425 |
| rs3087425 | |
| pharmgkb | rs3087425 |
| gwascentral | rs3087425 |
| openSNP | rs3087425 |
| 23andMe | rs3087425 |
| SNPshot | rs3087425 |
| SNPdbe | rs3087425 |
| MSV3d | rs3087425 |
| GWAS Ctlg | rs3087425 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 26690424
] Association of the rs1346044 Polymorphism of the Werner Syndrome Gene RECQL2 with Increased Risk and Premature Onset of Breast Cancer.
| ClinVar | |
|---|---|
| Risk | rs3087425(T;T) |
| Alt | rs3087425(T;T) |
| Reference | Rs3087425(C;C) |
| Significance | Other |
| Disease | Werner syndrome not specified |
| Variation | info |
| Gene | WRN |
| CLNDBN | Werner syndrome not specified |
| Reversed | 0 |
| HGVS | NC_000008.10:g.30977810C>T |
| CLNSRC | UniProtKB (protein) |
| CLNACC | RCV000032137.2, RCV000122280.2, |
