rs773906955
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (A;G) | 6 | Ovarian cancer susceptibility |
| (G;G) | 0 | common in clinvar |
| Make rs773906955(A;A) |
| Reference | GRCh38.p2 38.2/147 |
| Chromosome | 17 |
| Position | 35107026 |
| Gene | RAD51D, RAD51L3-RFFL |
| is a | snp |
| is | mentioned by |
| dbSNP | rs773906955 |
| dbSNP (classic) | rs773906955 |
| ClinGen | rs773906955 |
| ebi | rs773906955 |
| HLI | rs773906955 |
| Exac | rs773906955 |
| Gnomad | rs773906955 |
| Varsome | rs773906955 |
| LitVar | rs773906955 |
| Map | rs773906955 |
| PheGenI | rs773906955 |
| Biobank | rs773906955 |
| 1000 genomes | rs773906955 |
| hgdp | rs773906955 |
| ensembl | rs773906955 |
| geneview | rs773906955 |
| scholar | rs773906955 |
| rs773906955 | |
| pharmgkb | rs773906955 |
| gwascentral | rs773906955 |
| openSNP | rs773906955 |
| 23andMe | rs773906955 |
| SNPshot | rs773906955 |
| SNPdbe | rs773906955 |
| MSV3d | rs773906955 |
| GWAS Ctlg | rs773906955 |
| Max Magnitude | 6 |
| ClinVar | |
|---|---|
| Risk | rs773906955(A;A) |
| Alt | rs773906955(A;A) |
| Reference | Rs773906955(G;G) |
| Significance | Pathogenic |
| Disease | Hereditary cancer-predisposing syndrome |
| Variation | info |
| Gene | RAD51D RAD51L3-RFFL |
| CLNDBN | Hereditary cancer-predisposing syndrome |
| Reversed | 0 |
| HGVS | NC_000017.10:g.33434045G>A |
| CLNSRC | |
| CLNACC | RCV000215616.1, |
