Variant (rsID / SNP)

rs80359811

rs80359811 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to BRCA2. Location: chromosome 13, position 32,972,388. Clinical significance in the table: Benign.

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Reference-table entries

BRCA2Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 13:32972388
Cytoband: 13q13.1
HGVS: NM_000059.4(BRCA2):c.9738C>T (p.Ala3246=)
Allele change: Synonymous_A3246A

Associated conditions / phenotypes

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

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.