Gene entry
DNAH9
dynein axonemal heavy chain 9
- Chromosome
- 17
- Cytoband
- 17p12
- Variants (rsID)
- 128
DNAH9 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 17 (region 17p12). Its official name is “dynein axonemal heavy chain 9”. The reference table lists 128 variants (rsID) for this gene.
Clinically classified variants
7 reference-table entries with clinical significance.
- rs11078022Benignsingle nucleotide variantCiliary dyskinesia, primary, 40
- rs1990236Benignsingle nucleotide variant
- rs3744578Benignsingle nucleotide variantCiliary dyskinesia, primary, 40
- rs3744581Benignsingle nucleotide variantCiliary dyskinesia, primary, 40
- rs61740059Benignsingle nucleotide variant
- rs61744697Benignsingle nucleotide variant
- rs8070256Benignsingle nucleotide variantCiliary dyskinesia, primary, 40
Other listed variants
- rs740361
- rs887233
- rs1010797
- rs2018572
- rs2079719
- rs2190615
- rs2286300
- rs2286301
- rs2322053
- rs3744583
- rs3815269
- rs7225157
- rs7225975
- rs8065377
- rs8070501
- rs8074656
- rs8080946
- rs8081898
- rs9303041
- rs9889340
- rs9892829
- rs9894590
- rs9895370
- rs9903317
- rs9908085
- rs10445247
- rs10521187
- rs11649836
- rs11651009
- rs11871037
- rs12449769
- rs12453561
- rs12603082
- rs12709292
- rs12936449
- rs12937846
- rs12940825
- rs12945361
- rs12946617
- rs12946763
- rs16945138
- rs17599639
- rs56924590
- rs57240335
- rs61739481
- rs62060833
- rs62061841
- rs62063192
- rs67496656
- rs72810889
- rs72813306
- rs73975030
- rs74610583
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.