Variant (rsID / SNP)

rs587781689

rs587781689 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to BRCA2. Location: chromosome 13, position 32,944,591. Clinical significance in the table: Pathogenic.

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Reference-table entries

BRCA2Pathogenic

Clinical significance (as recorded): Pathogenic
Variant type: Deletion
Chromosome / position: 13:32944591
Cytoband: 13q13.1
HGVS: NM_000059.4(BRCA2):c.8384_8395del (p.Phe2795_Arg2799delinsTer)

Associated conditions / phenotypes

Hereditary cancer-predisposing syndrome|Breast-ovarian cancer, familial, susceptibility to, 2

Public references

dbSNP
ClinVar
Ensembl
gnomAD

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.