Gene entry
DNAAF3
dynein axonemal assembly factor 3
- Chromosome
- 19
- Cytoband
- 19q13.42
- Variants (rsID)
- 9
DNAAF3 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 19 (region 19q13.42). Its official name is “dynein axonemal assembly factor 3”. The reference table lists 9 variants (rsID) for this gene.
Clinically classified variants
9 reference-table entries with clinical significance.
- rs146442289Benignsingle nucleotide variantPrimary ciliary dyskinesia
- rs150362958Benignsingle nucleotide variantPrimary ciliary dyskinesia
- rs2365725Benignsingle nucleotide variantDilated Cardiomyopathy, Recessive|Hypertrophic cardiomyopathy|Familial restrictive cardiomyopathy|Primary ciliary dyskinesia|Familial Hypertrophic Cardiomyopathy with Wolff-Parkinson-White Syndrome|Primary ciliary dyskinesia 2
- rs3848618Benignsingle nucleotide variantHypertrophic cardiomyopathy|Familial Hypertrophic Cardiomyopathy with Wolff-Parkinson-White Syndrome|Dilated Cardiomyopathy, Recessive|Primary ciliary dyskinesia|Familial restrictive cardiomyopathy
- rs58824375Benignsingle nucleotide variantFamilial Hypertrophic Cardiomyopathy with Wolff-Parkinson-White Syndrome|Familial restrictive cardiomyopathy|Hypertrophic cardiomyopathy|Dilated Cardiomyopathy, Recessive|Primary ciliary dyskinesia
- rs890871Benignsingle nucleotide variantHypertrophic cardiomyopathy|Familial Hypertrophic Cardiomyopathy with Wolff-Parkinson-White Syndrome|Familial restrictive cardiomyopathy|Dilated Cardiomyopathy, Recessive|Primary ciliary dyskinesia
- rs200775946Conflicting interpretationssingle nucleotide variantPrimary ciliary dyskinesia
- rs201986299Conflicting interpretationsDeletionPrimary ciliary dyskinesia
- rs71367156Likely benignsingle nucleotide variantPrimary ciliary dyskinesia
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.