rs745677716
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 0 | common in clinvar |
| Make rs745677716(A;G) |
| Make rs745677716(G;G) |
| Reference | GRCh38.p2 38.2/144 |
| Chromosome | 11 |
| Position | 94445808 |
| Gene | MRE11A |
| is a | snp |
| is | mentioned by |
| dbSNP | rs745677716 |
| dbSNP (classic) | rs745677716 |
| ClinGen | rs745677716 |
| ebi | rs745677716 |
| HLI | rs745677716 |
| Exac | rs745677716 |
| Gnomad | rs745677716 |
| Varsome | rs745677716 |
| LitVar | rs745677716 |
| Map | rs745677716 |
| PheGenI | rs745677716 |
| Biobank | rs745677716 |
| 1000 genomes | rs745677716 |
| hgdp | rs745677716 |
| ensembl | rs745677716 |
| geneview | rs745677716 |
| scholar | rs745677716 |
| rs745677716 | |
| pharmgkb | rs745677716 |
| gwascentral | rs745677716 |
| openSNP | rs745677716 |
| 23andMe | rs745677716 |
| SNPshot | rs745677716 |
| SNPdbe | rs745677716 |
| MSV3d | rs745677716 |
| GWAS Ctlg | rs745677716 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs745677716(G;G) |
| Alt | rs745677716(G;G) |
| Reference | Rs745677716(A;A) |
| Significance | Probable-Pathogenic |
| Disease | Hereditary cancer-predisposing syndrome |
| Variation | info |
| Gene | MRE11A |
| CLNDBN | Hereditary cancer-predisposing syndrome |
| Reversed | 0 |
| HGVS | NC_000011.9:g.94178974A>G |
| CLNSRC | |
| CLNACC | RCV000166874.2, |
