Variant (rsID / SNP)
rs183521702
rs183521702 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DNAH11. Location: chromosome 7, position 21,641,054. 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
- 7:21641054
- Cytoband
- 7p15.3
- HGVS
- NM_001277115.2(DNAH11):c.3466G>A (p.Gly1156Arg)
- Allele change
- Missense_G1156R
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.