rs80359258
From SNPedia
| Orientation | plus |
| Geno | Mag | Summary |
|---|---|---|
| (-;A) | 1.9 | BRCA2 variant of uncertain significance, perhaps benign |
| (I;I) | 0 | common genotype |
| Make rs80359258(-;-) |
| Make rs80359258(A;A) |
| Reference | GRCh38.p7 38.3/151 |
| Chromosome | 13 |
| Position | 32398689 |
| Gene | BRCA2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs80359258 |
| dbSNP (classic) | rs80359258 |
| ClinGen | rs80359258 |
| ebi | rs80359258 |
| HLI | rs80359258 |
| Exac | rs80359258 |
| Gnomad | rs80359258 |
| Varsome | rs80359258 |
| LitVar | rs80359258 |
| Map | rs80359258 |
| PheGenI | rs80359258 |
| Biobank | rs80359258 |
| 1000 genomes | rs80359258 |
| hgdp | rs80359258 |
| ensembl | rs80359258 |
| geneview | rs80359258 |
| scholar | rs80359258 |
| rs80359258 | |
| pharmgkb | rs80359258 |
| gwascentral | rs80359258 |
| openSNP | rs80359258 |
| 23andMe | rs80359258 |
| SNPshot | rs80359258 |
| SNPdbe | rs80359258 |
| MSV3d | rs80359258 |
| GWAS Ctlg | rs80359258 |
| Merged from | Rs746515020 |
| Max Magnitude | 1.9 |
aka c.10176delA; annotated as likely to be benign or as a variant of uncertain significance in ClinVar
