Genetics University — Research, Education, Medical Genetics
Knowledge Hub

Variant (rsID / SNP)

rs28897728

BRCA2

rs28897728 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to BRCA2. Location: chromosome 13, position 32,913,077. Clinical significance in the table: Benign.

ShareE-MailWhatsAppLinkedInXFacebookTelegram

Reference-table entries

BRCA2Benign
Clinical significance (as recorded)
Benign
Variant type
single nucleotide variant
Chromosome / position
13:32913077
Cytoband
13q13.1
HGVS
NM_000059.4(BRCA2):c.4585G>A (p.Gly1529Arg)
Allele change
Missense_G1529R

Associated conditions / phenotypes

Hereditary breast ovarian cancer syndrome|Breast-ovarian cancer, familial, susceptibility to, 2|Breast and/or ovarian cancer|Hereditary cancer-predisposing syndrome|Fanconi anemia complementation group D1

Public references

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