rs80359195
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 0 | common in clinvar |
| Make rs80359195(A;C) |
| Make rs80359195(C;C) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 13 |
| Position | 32394707 |
| Gene | BRCA2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs80359195 |
| dbSNP (classic) | rs80359195 |
| ClinGen | rs80359195 |
| ebi | rs80359195 |
| HLI | rs80359195 |
| Exac | rs80359195 |
| Gnomad | rs80359195 |
| Varsome | rs80359195 |
| LitVar | rs80359195 |
| Map | rs80359195 |
| PheGenI | rs80359195 |
| Biobank | rs80359195 |
| 1000 genomes | rs80359195 |
| hgdp | rs80359195 |
| ensembl | rs80359195 |
| geneview | rs80359195 |
| scholar | rs80359195 |
| rs80359195 | |
| pharmgkb | rs80359195 |
| gwascentral | rs80359195 |
| openSNP | rs80359195 |
| 23andMe | rs80359195 |
| SNPshot | rs80359195 |
| SNPdbe | rs80359195 |
| MSV3d | rs80359195 |
| GWAS Ctlg | rs80359195 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs80359195(C;C) rs80359195(G;G) rs80359195(T;T) |
| Alt | rs80359195(C;C) rs80359195(G;G) rs80359195(T;T) |
| Reference | Rs80359195(A;A) |
| Significance | Other |
| Disease | Hereditary breast and ovarian cancer syndrome Breast-ovarian cancer Hereditary cancer-predisposing syndrome not specified |
| Variation | info |
| Gene | BRCA2 |
| CLNDBN | Hereditary breast and ovarian cancer syndrome Breast-ovarian cancer, familial 2 Hereditary cancer-predisposing syndrome not specified |
| Reversed | 0 |
| HGVS | NC_000013.10:g.32968844A>C; NC_000013.10:g.32968844A>G; NC_000013.10:g.32968844A>T |
| CLNSRC | ClinVar Ambry Genetics |
| CLNACC | RCV000045773.3, RCV000077465.3, RCV000045774.4, RCV000077466.5, RCV000131684.3, RCV000424310.1, RCV000077039.2, RCV000167271.1, RCV000483136.1, |
