rs774440500
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (-;-) | 0 | common in clinvar |
| Make rs774440500(-;T) |
| Make rs774440500(T;T) |
| Reference | GRCh38.p2 38.2/144 |
| Chromosome | 11 |
| Position | 94464115 |
| Gene | MRE11A |
| is a | snp |
| is | mentioned by |
| dbSNP | rs774440500 |
| dbSNP (classic) | rs774440500 |
| ClinGen | rs774440500 |
| ebi | rs774440500 |
| HLI | rs774440500 |
| Exac | rs774440500 |
| Gnomad | rs774440500 |
| Varsome | rs774440500 |
| LitVar | rs774440500 |
| Map | rs774440500 |
| PheGenI | rs774440500 |
| Biobank | rs774440500 |
| 1000 genomes | rs774440500 |
| hgdp | rs774440500 |
| ensembl | rs774440500 |
| geneview | rs774440500 |
| scholar | rs774440500 |
| rs774440500 | |
| pharmgkb | rs774440500 |
| gwascentral | rs774440500 |
| openSNP | rs774440500 |
| 23andMe | rs774440500 |
| SNPshot | rs774440500 |
| SNPdbe | rs774440500 |
| MSV3d | rs774440500 |
| GWAS Ctlg | rs774440500 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs774440500(T;T) |
| Alt | rs774440500(T;T) |
| Reference | Rs774440500(-;-) |
| Significance | Pathogenic |
| Disease | Hereditary cancer-predisposing syndrome |
| Variation | info |
| Gene | MRE11A |
| CLNDBN | Hereditary cancer-predisposing syndrome |
| Reversed | 0 |
| HGVS | NC_000011.9:g.94197282dupT |
| CLNSRC | |
| CLNACC | RCV000163829.1, |
