Variant (rsID / SNP)

rs206076

rs206076 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to BRCA2. Location: chromosome 13, position 32,915,005. The table records no clinical significance for this variant.

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Reference-table entries

BRCA2Not classified

Variant type: single nucleotide variant
Chromosome / position: 13:32915005
Cytoband: 13q13.1
HGVS: NM_000059.4(BRCA2):c.6513= (p.Val2171=)
Allele change: Synonymous_V2171V

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.