Variant (rsID / SNP)
rs28363317
rs28363317 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RAD51C. Location: chromosome 17, position 56,798,128. Clinical significance in the table: Benign/Likely benign.
Reference-table entries
RAD51CBenign
- Clinical significance (as recorded)
- Benign/Likely benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 17:56798128
- Cytoband
- 17q22
- HGVS
- NM_058216.3(RAD51C):c.859A>G (p.Thr287Ala)
- Allele change
- Silent
Associated conditions / phenotypes
Fanconi anemia complementation group O|Hereditary cancer-predisposing syndrome|Fanconi anemia|Breast and Ovarian Cancer Susceptibility|Breast-ovarian cancer, familial, susceptibility to, 3|Malignant tumor of breast|Hereditary breast ovarian cancer syndrome|Breast and/or ovarian cancer
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.