Variant (rsID / SNP)
rs886062182
rs886062182 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DNAH11. Location: chromosome 7, position 21,857,839. Clinical significance in the table: Conflicting interpretations of pathogenicity.
Reference-table entries
DNAH11Conflicting interpretations
- Clinical significance (as recorded)
- Conflicting interpretations of pathogenicity
- Variant type
- single nucleotide variant
- Chromosome / position
- 7:21857839
- Cytoband
- 7p15.3
- HGVS
- NM_001277115.2(DNAH11):c.10573T>C (p.Leu3525=)
- Allele change
- Synonymous_L3525L
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.