Variant (rsID / SNP)
rs999737
rs999737 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RAD51B. Location: chromosome 14, position 69,034,682. Clinical significance in the table: Benign.
Reference-table entries
RAD51BBenign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 14:69034682
- Cytoband
- 14q24.1
- HGVS
- NM_133509.5(RAD51B):c.1037-26520C>T
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.