rs372000848
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs372000848(A;A) |
| Make rs372000848(A;G) |
| Reference | GRCh38.p2 38.2/147 |
| Chromosome | 11 |
| Position | 94470575 |
| Gene | MRE11A |
| is a | snp |
| is | mentioned by |
| dbSNP | rs372000848 |
| dbSNP (classic) | rs372000848 |
| ClinGen | rs372000848 |
| ebi | rs372000848 |
| HLI | rs372000848 |
| Exac | rs372000848 |
| Gnomad | rs372000848 |
| Varsome | rs372000848 |
| LitVar | rs372000848 |
| Map | rs372000848 |
| PheGenI | rs372000848 |
| Biobank | rs372000848 |
| 1000 genomes | rs372000848 |
| hgdp | rs372000848 |
| ensembl | rs372000848 |
| geneview | rs372000848 |
| scholar | rs372000848 |
| rs372000848 | |
| pharmgkb | rs372000848 |
| gwascentral | rs372000848 |
| openSNP | rs372000848 |
| 23andMe | rs372000848 |
| SNPshot | rs372000848 |
| SNPdbe | rs372000848 |
| MSV3d | rs372000848 |
| GWAS Ctlg | rs372000848 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs372000848(A;A) |
| Alt | rs372000848(A;A) |
| Reference | Rs372000848(G;G) |
| Significance | Probable-Pathogenic |
| Disease | Hereditary cancer-predisposing syndrome not provided |
| Variation | info |
| Gene | MRE11A |
| CLNDBN | Hereditary cancer-predisposing syndrome not provided |
| Reversed | 0 |
| HGVS | NC_000011.9:g.94203741G>A |
| CLNSRC | UniProtKB (protein) |
| CLNACC | RCV000115925.10, RCV000212563.1, |
