Sensitive

Meniere's disease (PheCode 386.1)

near RNU6-832P · rs979245270

Where this position leads

Condition: Meniere's Disease

rs979245270 Condition: Meniere's Disease Meniere's Disease Condition rs979245270 rs979245270 near RNU6-83…

What the study found

Who was studied 232 Hispanic or Latin American cases, 59,553 Hispanic or Latin American controls, 2,074 European ancestry cases, 448,199 European ancestry controls.

The effect Each copy of the G allele shifted the measure 4.1 lower (95% confidence interval 4.09-4.11); p = 2 × 10−11.

How common The G allele had a frequency of about 100% in the people studied.

Where it sits Chromosome 7, band 7q11.22 — between genes, 9.9 kb from RNU6-832P.

What each result means

A/A Published research associates this genotype with typical/baseline likelihood of Meniere's disease (PheCode 386.1) — no copies of the reported risk allele.
A/G Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Meniere's disease (PheCode 386.1).
G/G Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Meniere's disease (PheCode 386.1) compared to the general population.
Source

Questions about rs979245270

What is rs979245270?

rs979245270 is a single position in the genome, in or near the near RNU6-832P gene. Published research associates it with meniere's disease (phecode 386.1). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs979245270 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 rs979245270 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 rs979245270 come from?

GWAS Catalog, Science (New York, N.Y.) 2024, PMID:39024449. 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.

Meniere's disease (PheCode 386.1) (rs979245270). MyGeneLog™. https://www.mygenelog.com/variants/rs979245270

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