rs779269083
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| Make rs779269083(A;A) |
| Make rs779269083(A;C) |
| Reference | GRCh38.p2 38.2/147 |
| Chromosome | 11 |
| Position | 94486009 |
| Gene | MRE11A |
| is a | snp |
| is | mentioned by |
| dbSNP | rs779269083 |
| dbSNP (classic) | rs779269083 |
| ClinGen | rs779269083 |
| ebi | rs779269083 |
| HLI | rs779269083 |
| Exac | rs779269083 |
| Gnomad | rs779269083 |
| Varsome | rs779269083 |
| LitVar | rs779269083 |
| Map | rs779269083 |
| PheGenI | rs779269083 |
| Biobank | rs779269083 |
| 1000 genomes | rs779269083 |
| hgdp | rs779269083 |
| ensembl | rs779269083 |
| geneview | rs779269083 |
| scholar | rs779269083 |
| rs779269083 | |
| pharmgkb | rs779269083 |
| gwascentral | rs779269083 |
| openSNP | rs779269083 |
| 23andMe | rs779269083 |
| SNPshot | rs779269083 |
| SNPdbe | rs779269083 |
| MSV3d | rs779269083 |
| GWAS Ctlg | rs779269083 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs779269083(A;A) rs779269083(T;T) |
| Alt | rs779269083(A;A) rs779269083(T;T) |
| Reference | Rs779269083(C;C) |
| Significance | Other |
| Disease | Hereditary cancer-predisposing syndrome |
| Variation | info |
| Gene | MRE11A |
| CLNDBN | Hereditary cancer-predisposing syndrome |
| Reversed | 0 |
| HGVS | NC_000011.9:g.94219175C>A |
| CLNSRC | |
| CLNACC | RCV000210166.1, |
