rs273899696
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (A;C) | 6 | BRCA1 variant considered pathogenic for breast cancer |
| (C;C) | 0 | common in clinvar |
| Make rs273899696(A;A) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 17 |
| Position | 43092505 |
| Gene | BRCA1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs273899696 |
| dbSNP (classic) | rs273899696 |
| ClinGen | rs273899696 |
| ebi | rs273899696 |
| HLI | rs273899696 |
| Exac | rs273899696 |
| Gnomad | rs273899696 |
| Varsome | rs273899696 |
| LitVar | rs273899696 |
| Map | rs273899696 |
| PheGenI | rs273899696 |
| Biobank | rs273899696 |
| 1000 genomes | rs273899696 |
| hgdp | rs273899696 |
| ensembl | rs273899696 |
| geneview | rs273899696 |
| scholar | rs273899696 |
| rs273899696 | |
| pharmgkb | rs273899696 |
| gwascentral | rs273899696 |
| openSNP | rs273899696 |
| 23andMe | rs273899696 |
| SNPshot | rs273899696 |
| SNPdbe | rs273899696 |
| MSV3d | rs273899696 |
| GWAS Ctlg | rs273899696 |
| Max Magnitude | 6 |
| ClinVar | |
|---|---|
| Risk | rs273899696(A;A) |
| Alt | rs273899696(A;A) |
| Reference | Rs273899696(C;C) |
| Significance | Pathogenic |
| Disease | Familial cancer of breast Breast-ovarian cancer |
| Variation | info |
| Gene | BRCA1 |
| CLNDBN | Familial cancer of breast Breast-ovarian cancer, familial 1 |
| Reversed | 1 |
| HGVS | NC_000017.10:g.41244522G>T |
| CLNSRC | ClinVar |
| CLNACC | RCV000048052.2, RCV000111985.2, |
