rs587776427
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (-;-) | 7 | Fanconi anemia, complementation group N |
| (-;GT) | 3 | significantly increased risk of breast cancer |
| (GT;GT) | 0 | common in clinvar |
| Reference | GRCh38 38.1/142 |
| Chromosome | 16 |
| Position | 23603522 |
| Gene | PALB2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs587776427 |
| dbSNP (classic) | rs587776427 |
| ClinGen | rs587776427 |
| ebi | rs587776427 |
| HLI | rs587776427 |
| Exac | rs587776427 |
| Gnomad | rs587776427 |
| Varsome | rs587776427 |
| LitVar | rs587776427 |
| Map | rs587776427 |
| PheGenI | rs587776427 |
| Biobank | rs587776427 |
| 1000 genomes | rs587776427 |
| hgdp | rs587776427 |
| ensembl | rs587776427 |
| geneview | rs587776427 |
| scholar | rs587776427 |
| rs587776427 | |
| pharmgkb | rs587776427 |
| gwascentral | rs587776427 |
| openSNP | rs587776427 |
| 23andMe | rs587776427 |
| SNPshot | rs587776427 |
| SNPdbe | rs587776427 |
| MSV3d | rs587776427 |
| GWAS Ctlg | rs587776427 |
| Max Magnitude | 7 |
| ClinVar | |
|---|---|
| Risk | Rs587776427(-;-) |
| Alt | Rs587776427(-;-) |
| Reference | Rs587776427(GT;GT) |
| Significance | Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | PALB2 |
| CLNDBN | not provided |
| Reversed | 1 |
| HGVS | NC_000016.9:g.23614843_23614844delAC |
| CLNSRC | ClinVar |
| CLNACC | RCV000133489.1, |
