Variant (rsID / SNP)

rs201986299

rs201986299 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DNAAF3. Location: chromosome 19, position 55,673,662. Clinical significance in the table: Conflicting interpretations of pathogenicity.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

DNAAF3Conflicting interpretations

Clinical significance (as recorded): Conflicting interpretations of pathogenicity
Variant type: Deletion
Chromosome / position: 19:55673662
Cytoband: 19q13.42
HGVS: NM_001256715.2(DNAAF3):c.323-4del

Associated conditions / phenotypes

Primary ciliary dyskinesia

Public references

dbSNP
ClinVar
Ensembl
gnomAD

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.