EYA1 · rs145240113
Where this position leads
Condition: Ménière's Disease
Strength of the evidence
Its strongest genetic-study result is p = 10−9, with 1 associations in the GWAS Catalog.
4: ClinVar disease-causing, reviewed by an expert panel or a guideline (3–4 stars). 3: ClinVar, several labs agreeing (2 stars), or a genetic study at p ≤ 10−50. 2: ClinVar from one lab (1 star), or p ≤ 10−20. 1: ClinVar submitted without criteria (0 stars), or genome-wide significance (p ≤ 5×10−8). The higher of the two counts. It says how solid the evidence is, not whether it matters for a particular person.
What the study found
Who was studied 7,303 European ancestry cases, 1,564,233 European ancestry controls, 1,301 East Asian ancestry cases, 187,114 East Asian ancestry controls, 296 Hispanic or Latin American cases, 129,993 Hispanic or Latin American controls, 69 cases, 81,202 controls.
The effect The reported allele is G; the catalogue records no effect size ; p = 1 × 10−9.
How common The G allele had a frequency of about 10% in the people studied.
Where it sits Chromosome 8, band 8q13.3 — in an intron of EYA1.
rs145240113 is a single position in the genome, in or near the EYA1 gene. Published research associates it with meniere's disease. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
On MyGeneLog this position is linked to Ménière's Disease. The research behind each link, and its sources, are set out on that condition page.
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.
GWAS Catalog, American journal of human genetics 2026, PMID:42302782. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
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.
Meniere's disease (rs145240113). MyGeneLog™. https://www.mygenelog.com/variants/rs145240113