Trait
Chronic bronchitis
Chronic inflammation of the bronchi.
Summary
Reference genomeGRCh38hg38
Positions on gene and variant pages follow this choice, in this browser.
Read the genes linked to Chronic bronchitis, and the rest of your genome, with one test.
From $449Free shipping · Results in 6–8 weeks
Get my Genome Test30 genes linked to Chronic bronchitis
Changes in these genes cause rare conditions in which Chronic bronchitis is seen. Most people with this trait have none of those conditions, and a gene on this list says nothing about anyone's own genome.
| Gene | How often it is seen | Conditions |
|---|---|---|
| CCDC39coiled-coil domain 39 molecular ruler complex subunit | Always | In 1 condition |
| CCDC40coiled-coil domain 40 molecular ruler complex subunit | Always | In 1 condition |
| DNAH7dynein axonemal heavy chain 7 | Always | In 1 condition |
| HYDINHYDIN axonemal central pair apparatus protein | Always | In 1 condition |
| IFT140intraflagellar transport 140 | Always | In 1 condition |
| POLD1DNA polymerase delta 1, catalytic subunit | Always | In 1 condition |
| RAC2Rac family small GTPase 2 | Always | In 1 condition |
| TAP2transporter 2, ATP binding cassette subfamily B member | Always | In 1 condition |
| UBAP2Lubiquitin associated protein 2 like | Always | In 1 condition |
| DNAAF11dynein axonemal assembly factor 11 | Very often (80–99%) | In 1 condition |
| ALMS1ALMS1 centrosome and basal body associated protein | Often (30–79%) | In 1 condition |
| DNAAF5dynein axonemal assembly factor 5 | Often (30–79%) | In 1 condition |
| ODAD2outer dynein arm docking complex subunit 2 | Often (30–79%) | In 1 condition |
| CARMIL2capping protein regulator and myosin 1 linker 2 | Sometimes (5–29%) | In 1 condition |
| DNAAF4dynein axonemal assembly factor 4 | Sometimes (5–29%) | In 1 condition |
| GUSBglucuronidase beta | Sometimes (5–29%) | In 1 condition |
| IFT54intraflagellar transport 54 | Sometimes (5–29%) | In 1 condition |
| ODAD3outer dynein arm docking complex subunit 3 | Sometimes (5–29%) | In 1 condition |
| RSPH4Aradial spoke head component 4A | Sometimes (5–29%) | In 1 condition |
| SERPINA1serpin family A member 1 | Sometimes (5–29%) | In 1 condition |
| CFAP298cilia and flagella associated protein 298 | Not recorded | In 1 condition |
| CFTRCF transmembrane conductance regulator | Not recorded | In 1 condition |
| DNMT3BDNA methyltransferase 3 beta | Not recorded | In 1 condition |
| DRC2dynein regulatory complex subunit 2 | Not recorded | In 1 condition |
| SCNN1Asodium channel epithelial 1 subunit alpha | Not recorded | In 1 condition |
| SCNN1Bsodium channel epithelial 1 subunit beta | Not recorded | In 1 condition |
| SCNN1Gsodium channel epithelial 1 subunit gamma | Not recorded | In 1 condition |
| SPAG1sperm associated antigen 1 | Not recorded | In 1 condition |
| ZBTB24zinc finger and BTB domain containing 24 | Not recorded | In 1 condition |
| ZMYND10zinc finger MYND-type containing 10 | Not recorded | In 1 condition |
How often is among people with one of the gene's conditions, the most often across them, as the Human Phenotype Ontology records it. These pages describe traits and the research behind them; they are not a diagnosis, and a doctor or genetic counsellor is the person to ask about symptoms.
Broader traits
Where this comes from
- The Human Phenotype Ontology, release 2026-09-01: the trait, its names, its definition and the genes linked to it. Find out more at hpo.jax.org.
- Data release 2026.10.16-c6eea6bf.
One test. A lifetime of answers.
From $449Free shipping · Results in 6–8 weeks