Variant (rsID / SNP)
rs28897696
rs28897696 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to BRCA1. Location: chromosome 17, position 41,215,920. Clinical significance in the table: Uncertain significance.
Reference-table entries
BRCA1Uncertain significance
- Clinical significance (as recorded)
- Uncertain significance
- Variant type
- single nucleotide variant
- Chromosome / position
- 17:41215920
- Cytoband
- 17q21.31
- HGVS
- NM_007294.4(BRCA1):c.5123C>T (p.Ala1708Val)
- Allele change
- Silent
Associated conditions / phenotypes
Breast-ovarian cancer, familial, susceptibility to, 1|Hereditary breast ovarian cancer syndrome|Hereditary cancer-predisposing syndrome|Breast and/or ovarian cancer|Malignant tumor of breast|Familial cancer of breast
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.