Variant (rsID / SNP)
rs1484076591
rs1484076591 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to BRCA1. Location: chromosome 17, position 41,244,465. Clinical significance in the table: Pathogenic.
Reference-table entries
BRCA1Pathogenic
- Clinical significance (as recorded)
- Pathogenic
- Variant type
- Deletion
- Chromosome / position
- 17:41244465
- Cytoband
- 17q21.31
- HGVS
- NM_007294.4(BRCA1):c.3083del (p.Arg1028fs)
Associated conditions / phenotypes
Hereditary cancer-predisposing syndrome
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.