Variant (rsID / SNP)
rs876659874
rs876659874 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RAD51C. Location: chromosome 17, position 56,801,410. Clinical significance in the table: Pathogenic/Likely pathogenic.
Reference-table entries
RAD51CPathogenic
- Clinical significance (as recorded)
- Pathogenic/Likely pathogenic
- Variant type
- single nucleotide variant
- Chromosome / position
- 17:56801410
- Cytoband
- 17q22
- HGVS
- NM_058216.3(RAD51C):c.914G>A (p.Trp305Ter)
- Allele change
- Silent
Associated conditions / phenotypes
Hereditary cancer-predisposing syndrome|Fanconi anemia complementation group O|Breast-ovarian cancer, familial, susceptibility to, 3|Fanconi anemia complementation group O|Breast-ovarian cancer, familial, susceptibility to, 3
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.