Variant (rsID / SNP)
rs397508994
rs397508994 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to BRCA1. Location: chromosome 17, position 41,244,873. The table records no clinical significance for this variant.
Reference-table entries
BRCA1Not classified
- Variant type
- single nucleotide variant
- Chromosome / position
- 17:41244873
- Cytoband
- 17q21.31
- HGVS
- NM_007294.4(BRCA1):c.2675T>C (p.Leu892Ser)
- Allele change
- Silent
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.