Variant (rsID / SNP)
rs79349285
rs79349285 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CCDC39, TTC14. Location: chromosome 3, position 180,332,134. Clinical significance in the table: Benign.
Reference-table entries
CCDC39Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 3:180332134
- Cytoband
- 3q26.33
- HGVS
- NM_181426.2(CCDC39):c.*575T>C
- Allele change
- Silent
Associated conditions / phenotypes
Primary ciliary dyskinesia 14
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.