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Variant (rsID / SNP)

rs768143929

BRCA2

rs768143929 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to BRCA2. Location: chromosome 13, position 32,910,840. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

BRCA2Conflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
13:32910840
Cytoband
13q13.1
HGVS
NM_000059.4(BRCA2):c.2348T>G (p.Val783Gly)
Allele change
Missense_V783G

Associated conditions / phenotypes

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

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.