Variant (rsID / SNP)
rs397507585
rs397507585 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to BRCA2. Location: chromosome 13, position 32,907,007. The table records no clinical significance for this variant.
Reference-table entries
BRCA2Not classified
- Variant type
- Insertion
- Chromosome / position
- 13:32907007
- Cytoband
- 13q13.1
- HGVS
- NM_000059.4(BRCA2):c.1392_1393insT (p.Val465fs)
Associated conditions / phenotypes
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.