Variant (rsID / SNP)
rs72657339
rs72657339 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DNAH11. Location: chromosome 7, position 21,737,718. Clinical significance in the table: Benign.
Reference-table entries
DNAH11Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 7:21737718
- Cytoband
- 7p15.3
- HGVS
- NM_001277115.2(DNAH11):c.6067A>G (p.Ile2023Val)
- Allele change
- Missense_I2023V
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.