Variant (rsID / SNP)

rs886040771

rs886040771 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to BRCA2. Location: chromosome 13, position 32,944,602. 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: 13:32944602
Cytoband: 13q13.1
HGVS: NM_000059.4(BRCA2):c.8395A>T (p.Arg2799Ter)
Allele change: Nonsense_R2799X

Associated conditions / phenotypes

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.