rs51526122
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs51526122(A;A) |
| Make rs51526122(A;G) |
| Make rs51526122(G;G) |
| Reference | GRCm38.p1 38.2/138 |
| Chromosome | 5 |
| Position | 56546164 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs51526122 |
| dbSNP (classic) | rs51526122 |
| ClinGen | rs51526122 |
| ebi | rs51526122 |
| HLI | rs51526122 |
| Exac | rs51526122 |
| Gnomad | rs51526122 |
| Varsome | rs51526122 |
| LitVar | rs51526122 |
| Map | rs51526122 |
| PheGenI | rs51526122 |
| Biobank | rs51526122 |
| 1000 genomes | rs51526122 |
| hgdp | rs51526122 |
| ensembl | rs51526122 |
| geneview | rs51526122 |
| scholar | rs51526122 |
| rs51526122 | |
| pharmgkb | rs51526122 |
| gwascentral | rs51526122 |
| openSNP | rs51526122 |
| 23andMe | rs51526122 |
| SNPshot | rs51526122 |
| SNPdbe | rs51526122 |
| MSV3d | rs51526122 |
| GWAS Ctlg | rs51526122 |
| Max Magnitude | 0 |
[PMID 25099575] Breast-Cancer Risk in Families with Mutations in PALB2
see also ClinVar (where clinical significance = pathogenic)
