Variant (rsID / SNP)

rs876660897

rs876660897 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to BRCA2. Location: chromosome 13, position 32,918,729. Clinical significance in the table: Likely benign.

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Reference-table entries

BRCA2Likely benign

Clinical significance (as recorded): Likely benign
Variant type: single nucleotide variant
Chromosome / position: 13:32918729
Cytoband: 13q13.1
HGVS: NM_000059.4(BRCA2):c.6876A>G (p.Glu2292=)
Allele change: Synonymous_E2292E

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.