Variant (rsID / SNP)
rs11571833
rs11571833 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to BRCA2. Location: chromosome 13, position 32,972,626. Clinical significance in the table: Benign.
Reference-table entries
BRCA2Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 13:32972626
- Cytoband
- 13q13.1
- HGVS
- NM_000059.4(BRCA2):c.9976A>T (p.Lys3326Ter)
- Allele change
- Nonsense_K3326X
Associated conditions / phenotypes
Breast-ovarian cancer, familial, susceptibility to, 2|Hereditary breast ovarian cancer syndrome|Hereditary cancer-predisposing syndrome|Breast and/or ovarian cancer|Malignant tumor of breast|Fanconi anemia complementation group D1|Familial cancer of breast
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.