rs10492396
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs10492396(A;A) |
| Make rs10492396(A;G) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 13 |
| Position | 32384750 |
| Gene | BRCA2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs10492396 |
| dbSNP (classic) | rs10492396 |
| ClinGen | rs10492396 |
| ebi | rs10492396 |
| HLI | rs10492396 |
| Exac | rs10492396 |
| Gnomad | rs10492396 |
| Varsome | rs10492396 |
| LitVar | rs10492396 |
| Map | rs10492396 |
| PheGenI | rs10492396 |
| Biobank | rs10492396 |
| 1000 genomes | rs10492396 |
| hgdp | rs10492396 |
| ensembl | rs10492396 |
| geneview | rs10492396 |
| scholar | rs10492396 |
| rs10492396 | |
| pharmgkb | rs10492396 |
| gwascentral | rs10492396 |
| openSNP | rs10492396 |
| 23andMe | rs10492396 |
| SNPshot | rs10492396 |
| SNPdbe | rs10492396 |
| MSV3d | rs10492396 |
| GWAS Ctlg | rs10492396 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 25243787
] Genetic variants in fanconi anemia pathway genes BRCA2 and FANCA predict melanoma survival
| ClinVar | |
|---|---|
| Risk | rs10492396(A;A) |
| Alt | rs10492396(A;A) |
| Reference | Rs10492396(G;G) |
| Significance | Non-pathogenic |
| Disease | Breast-ovarian cancer |
| Variation | info |
| Gene | BRCA2 |
| CLNDBN | Breast-ovarian cancer, familial 2 |
| Reversed | 0 |
| HGVS | NC_000013.10:g.32958887G>A |
| CLNSRC | |
| CLNACC | RCV000191814.1, |
