Variant (rsID / SNP)

rs776655838

rs776655838 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to BRCA2. Location: chromosome 13, position 32,911,987. 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: 13:32911987
Cytoband: 13q13.1
HGVS: NM_000059.4(BRCA2):c.3495T>C (p.His1165=)
Allele change: Synonymous_H1165H

Associated conditions / phenotypes

Hereditary cancer-predisposing syndrome|Hereditary breast ovarian cancer syndrome|Fanconi anemia complementation group D1|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.