1 81223Reads by AI crawlersClaude1ChatGPT0Google · Gemini0Perplexity0Meta AI2Microsoft · Copilot0Amazon2Apple0Others3Total8Counted by the name each crawler declares; requests found to be impersonating one are left out. Google · Gemini includes Googlebot, the search crawler whose index Google also uses for its AI features. Other search engines and bots are under Others.
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 × 10−17.
How common The G allele had a frequency of about 9% in the people studied.
Where it sits Chromosome 6, band 6q23.2 — in an intron of EYA4.
What each result means
A/APublished research associates this genotype with typical/baseline likelihood of Meniere's disease — no copies of the reported risk allele.
A/GPublished research associates this genotype (one copy of the reported risk allele) with an intermediate association with Meniere's disease.
G/GPublished research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Meniere's disease compared to the general population.
American journal of human genetics · 2026 · PMID 42302782 · open access
Questions about rs3777811
What is rs3777811?
rs3777811 is a single position in the genome, in or near the EYA4 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.
What conditions is rs3777811 linked to?
On MyGeneLog this position is linked to Meniere's Disease. The research behind each link, and its sources, are set out on that condition page.
Does having rs3777811 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 rs3777811 come from?
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.
1 81223Reads by AI crawlersClaude1ChatGPT0Google · Gemini0Perplexity0Meta AI2Microsoft · Copilot0Amazon2Apple0Others3Total8Counted by the name each crawler declares; requests found to be impersonating one are left out. Google · Gemini includes Googlebot, the search crawler whose index Google also uses for its AI features. Other search engines and bots are under Others.
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