Variant (rsID / SNP)
rs876658929
rs876658929 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to BRCA2. Location: chromosome 13, position 32,911,100. Clinical significance in the table: Pathogenic.
Reference-table entries
BRCA2Pathogenic
- Clinical significance (as recorded)
- Pathogenic
- Variant type
- Duplication
- Chromosome / position
- 13:32911100
- Cytoband
- 13q13.1
- HGVS
- NM_000059.4(BRCA2):c.2611dup (p.Ser871fs)
Associated conditions / phenotypes
Hereditary cancer-predisposing syndrome|Breast-ovarian cancer, familial, susceptibility to, 2
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.