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Variant (rsID / SNP)

rs397507411

BRCA2

rs397507411 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to BRCA2. Location: chromosome 13, position 32,950,869. Clinical significance in the table: Pathogenic.

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Reference-table entries

BRCA2Pathogenic
Clinical significance (as recorded)
Pathogenic
Variant type
single nucleotide variant
Chromosome / position
13:32950869
Cytoband
13q13.1
HGVS
NM_000059.4(BRCA2):c.8695C>T (p.Gln2899Ter)
Allele change
Nonsense_Q2899X

Associated conditions / phenotypes

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

Public references

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