Acute Laryngitis and Tracheitis, as genome-wide studies have reported it: 7 positions from 1 study, the largest recording 885 cases and 567,247 controls (African American or Afro-Caribbean ancestry, European ancestry). Built from the GWAS Catalog's records and rebuilt when a new position is reported; the figures are the studies'.
Acute Laryngitis and Tracheitis — filed in the GWAS Catalog as "Acute laryngitis and tracheitis (PheCode 465.4)" — is a condition this catalogue follows as its positions arrive. This page is assembled by MyGeneLog's own code from the catalogue's records and the studies' own listings: 7 positions from 1 study, and no sentence written by hand. It is rebuilt as new positions are reported, so what it says is what the records say today.
Verma A et al. 2024, in Science — Diversity and scale: Genetic architecture of 2068 traits in the VA Million Veteran Program. Sample in the catalogue's record: 885 cases and 567,247 controls (African American or Afro-Caribbean ancestry, European ancestry). The 7 positions on this page from it: rs536304276 (near ECM1P2), rs190677496 (near Y_RNA), rs138404838 (DLL1), rs142601420 (ABCA7), rs75738385 (near RPL35AP30), rs182096803 (near STARD13), rs545699183 (CCDC88C). PMID:39024449.
The catalogue maps the 7 positions to 7 genes: ECM1P2, Y_RNA, DLL1, ABCA7, RPL35AP30, STARD13, CCDC88C. That mapping says where a position sits, in a gene or beside one — not what it does. For what each study measured, follow its citation above.
Verma A et al. 2024 reported the smallest P value on this page — P = 8 × 10-14 — at rs536304276 near ECM1P2.
Association records say which positions differ, on average, between people with Acute Laryngitis and Tracheitis and people without. They do not describe the condition, say how common it is, or tell anyone what to do, so this page does not either. For a single position, open its variant page: it gives that study's record in fixed sentences, with ClinVar's where there is one.
A genotype does not diagnose Acute Laryngitis and Tracheitis; a clinician does. No guideline uses the 7 variants on this page to predict it, screen for it or confirm it.
Everything here comes from population-level association records, put together by code. Those records compare groups of people; they do not examine anyone, and they give no guidance on care. For symptoms, testing or treatment, ask a clinician.
What a 23andMe/AncestryDNA export or raw VCF can and can't tell you about Acute Laryngitis and Tracheitis comes down to these specific, well-studied positions — not a diagnosis.
near ECM1P2 · rs536304276
See detailed info →near Y_RNA · rs190677496
See detailed info →near RPL35AP30 · rs75738385
See detailed info →near STARD13 · rs182096803
See detailed info →Databases, guidelines and references
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Acute Laryngitis and Tracheitis. MyGeneLog™. https://www.mygenelog.com/conditions/acute-laryngitis-and-tracheitis
In the GWAS Catalog, Acute Laryngitis and Tracheitis is filed as "Acute laryngitis and tracheitis (PheCode 465.4)". Rather than define it, this page lists the genome-wide findings: 7 positions from 1 study, each with its study's sample and citation.
Genome-wide studies have reported 7 associated positions; the largest study behind this page recorded 885 cases and 567,247 controls (African American or Afro-Caribbean ancestry, European ancestry). Each common variant has a small effect, and an association in a population is not a cause in any one person.
The positions lie in or near 7 genes: ECM1P2, Y_RNA, DLL1, ABCA7, RPL35AP30, STARD13, CCDC88C. A mapped gene is the catalogue's location for a position, not a mechanism.
No. Each variant shifts the odds only slightly, and only on average across many people. No guideline predicts Acute Laryngitis and Tracheitis from a genotype; a clinician diagnoses it.
Free to reuse. This page's text is original writing from freely-available research, licensed CC BY 4.0 — reuse it, including commercially, with attribution to MyGeneLog™. It's general research-derived information, not medical advice or a diagnosis — see Terms of Use.