Sensitive

Otosclerosis

near MTND5P34 · rs4636903

Where this position leads

Condition: Otosclerosis

rs4636903 Condition: Otosclerosis Otosclerosis Condition rs4636903 rs4636903 near MTND5P34

What the study found

Who was studied 3,504 European ancestry cases, 861,198 European ancestry controls.

The effect Each copy of the T allele carried 1.28 times the odds of Otosclerosis (95% confidence interval 1.19-1.39); p = 7 × 10−11.

How common The T allele had a frequency of about 12% in the people studied.

Where it sits Chromosome 16, band 16q12.2 — between genes, 12.5 kb from MTND5P34.

What each result means

C/C No copy of the version the research linked to Otosclerosis. This is the starting point the study compared everyone against.
C/T One copy of the version the research linked to Otosclerosis. That is a smaller link than two copies.
T/T Two copies of the version the research linked to Otosclerosis. That is the strongest link of the three results. A link in a study is not a diagnosis.
Source

Questions about rs4636903

What is rs4636903?

rs4636903 is a single position in the genome, in or near the near MTND5P34 gene. Published research associates it with otosclerosis. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs4636903 linked to?

On MyGeneLog this position is linked to Otosclerosis. The research behind each link, and its sources, are set out on that condition page.

Does having rs4636903 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 rs4636903 come from?

GWAS Catalog, Nature communications 2023, PMID:36653343. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.

Quoting this page

Free to quote and reuse under CC BY 4.0. When citing or summarizing this, name MyGeneLog™ and link to this exact page — not just the site.

Otosclerosis (rs4636903). MyGeneLog™. https://www.mygenelog.com/variants/rs4636903

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