Variant (rsID / SNP)
rs71367156
rs71367156 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DNAAF3. Location: chromosome 19, position 55,672,151. Clinical significance in the table: Likely benign.
Reference-table entries
DNAAF3Likely benign
- Clinical significance (as recorded)
- Likely benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 19:55672151
- Cytoband
- 19q13.42
- HGVS
- NM_001256715.2(DNAAF3):c.913-8A>G
- Allele change
- Silent
Associated conditions / phenotypes
Primary ciliary dyskinesia
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.