rs799906
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (T;T) | 0 | common in clinvar |
| Make rs799906(C;C) |
| Make rs799906(C;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 17 |
| Position | 43126099 |
| Gene | BRCA1, NBR2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs799906 |
| dbSNP (classic) | rs799906 |
| ClinGen | rs799906 |
| ebi | rs799906 |
| HLI | rs799906 |
| Exac | rs799906 |
| Gnomad | rs799906 |
| Varsome | rs799906 |
| LitVar | rs799906 |
| Map | rs799906 |
| PheGenI | rs799906 |
| Biobank | rs799906 |
| 1000 genomes | rs799906 |
| hgdp | rs799906 |
| ensembl | rs799906 |
| geneview | rs799906 |
| scholar | rs799906 |
| rs799906 | |
| pharmgkb | rs799906 |
| gwascentral | rs799906 |
| openSNP | rs799906 |
| 23andMe | rs799906 |
| SNPshot | rs799906 |
| SNPdbe | rs799906 |
| MSV3d | rs799906 |
| GWAS Ctlg | rs799906 |
| GMAF | 0.4481 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 12466288
] Haplotype and linkage disequilibrium architecture for human cancer-associated genes.
| ClinVar | |
|---|---|
| Risk | rs799906(C;C) |
| Alt | rs799906(C;C) |
| Reference | Rs799906(T;T) |
| Significance | Non-pathogenic |
| Disease | Breast-ovarian cancer |
| Variation | info |
| Gene | NBR2 BRCA1 |
| CLNDBN | Breast-ovarian cancer, familial 1 |
| Reversed | 0 |
| HGVS | NC_000017.10:g.41278116T>C |
| CLNSRC | |
| CLNACC | RCV000191528.1, |
