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Stands on its own.
Nothing else here links to this position yet — but the page above is the point: what the
research found, what each genotype means, and where it came from, in language you can
read. Links to conditions, drugs and the senses appear automatically if we write them.
What the study found
Who was studied 121,934 European ancestry cases, 591,699 European ancestry controls.
The effect
Each copy of the G allele carried 0.96 times the odds of Age-related hearing impairment; p = 4 × 10−12.
Where it sits Chromosome 11, band 11p15.4 — in a non-coding transcript of TUB.
What each result means
A/ANo copy of the version the research linked to Age-related hearing impairment. This is the starting point the study compared everyone against.
A/GOne copy of the version the research linked to Age-related hearing impairment. That is a smaller link than two copies.
G/GTwo copies of the version the research linked to Age-related hearing impairment. That is the strongest link of the three results. A link in a study is not a diagnosis.
Communications biology · 2021 · PMID 34108613 · open access
Questions about rs55635402
What is rs55635402?
rs55635402 is a single position in the genome, in or near the TUB gene. Published research associates it with age-related hearing impairment. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs55635402 mean I will get this?
No. Common variants like this one move a probability slightly and, on their own, rarely decide anything about one person. Nothing on this page is a diagnosis, and health decisions should be made with a clinician who can see your whole picture.
Where does the information about rs55635402 come from?
GWAS Catalog, Communications biology 2021, PMID:34108613. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
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