Variant (rsID / SNP)

rs80359688

rs80359688 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to BRCA2. Location: chromosome 13, position 32,936,788. Clinical significance in the table: Pathogenic.

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Reference-table entries

BRCA2Pathogenic

Clinical significance (as recorded): Pathogenic
Variant type: Deletion
Chromosome / position: 13:32936788
Cytoband: 13q13.1
HGVS: NM_000059.4(BRCA2):c.7934del (p.Arg2645fs)

Associated conditions / phenotypes

Breast-ovarian cancer, familial, susceptibility to, 2|Hereditary cancer-predisposing syndrome|Hereditary breast ovarian cancer syndrome|Hereditary breast ovarian cancer syndrome|Fanconi anemia complementation group D1

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.