Variant (rsID / SNP)
rs17203442
rs17203442 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DNAH5. Location: chromosome 5, position 13,721,378. Clinical significance in the table: Benign.
Reference-table entries
DNAH5Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 5:13721378
- Cytoband
- 5p15.2
- HGVS
- NM_001369.3(DNAH5):c.12034-24T>C
- Allele change
- Silent
Associated conditions / phenotypes
Primary ciliary dyskinesia 3
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.