rs730881942
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs730881942(-;-) |
| Make rs730881942(-;G) |
| Reference | GRCh38.p2 38.2/144 |
| Chromosome | 17 |
| Position | 58692736 |
| Gene | RAD51C, TEX14 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs730881942 |
| dbSNP (classic) | rs730881942 |
| ClinGen | rs730881942 |
| ebi | rs730881942 |
| HLI | rs730881942 |
| Exac | rs730881942 |
| Gnomad | rs730881942 |
| Varsome | rs730881942 |
| LitVar | rs730881942 |
| Map | rs730881942 |
| PheGenI | rs730881942 |
| Biobank | rs730881942 |
| 1000 genomes | rs730881942 |
| hgdp | rs730881942 |
| ensembl | rs730881942 |
| geneview | rs730881942 |
| scholar | rs730881942 |
| rs730881942 | |
| pharmgkb | rs730881942 |
| gwascentral | rs730881942 |
| openSNP | rs730881942 |
| 23andMe | rs730881942 |
| SNPshot | rs730881942 |
| SNPdbe | rs730881942 |
| MSV3d | rs730881942 |
| GWAS Ctlg | rs730881942 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs730881942(-;-) |
| Alt | rs730881942(-;-) |
| Reference | Rs730881942(G;G) |
| Significance | Other |
| Disease | Breast-ovarian cancer Hereditary cancer-predisposing syndrome Fanconi anemia not provided |
| Variation | info |
| Gene | TEX14 RAD51C |
| CLNDBN | Breast-ovarian cancer, familial 3 Hereditary cancer-predisposing syndrome Fanconi anemia, complementation group O not provided |
| Reversed | 0 |
| HGVS | NC_000017.10:g.56770097delG |
| CLNSRC | OMIM Allelic Variant |
| CLNACC | RCV000024266.3, RCV000160936.3, RCV000205375.2, RCV000212931.1, |
