Variant (rsID / SNP)
rs886038038
rs886038038 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to BRCA1. Location: chromosome 17, position 41,222,962. Clinical significance in the table: Pathogenic.
Reference-table entries
BRCA1Pathogenic
- Clinical significance (as recorded)
- Pathogenic
- Variant type
- Deletion
- Chromosome / position
- 17:41222962
- Cytoband
- 17q21.31
- HGVS
- NM_007294.4(BRCA1):c.4969del (p.Gly1656_Leu1657insTer)
Associated conditions / phenotypes
Breast-ovarian cancer, familial, susceptibility to, 1
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.