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Variant (rsID / SNP)

rs757430441

BRCA2

rs757430441 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to BRCA2. Location: chromosome 13, position 32,906,524. 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
13:32906524
Cytoband
13q13.1
HGVS
NM_000059.4(BRCA2):c.909T>G (p.Ser303=)
Allele change
Synonymous_S303S

Associated conditions / phenotypes

Hereditary breast ovarian cancer syndrome|Hereditary cancer-predisposing syndrome|Fanconi anemia complementation group D1|Breast-ovarian cancer, familial, susceptibility to, 2|Malignant tumor of breast

Public references

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