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Early-onset myasthenia gravis

near RNU6-283P · rs2853986

Where this position leads

Condition: Myasthenia Gravis

rs2853986 Condition: Myasthenia Gravis Myasthenia Gravis Condition rs2853986 rs2853986 near RNU6-28…

What the study found

Who was studied 1,391 European ancestry early-onset cases, 22,407 European ancestry controls; replicated in 871 early-onset cases, 109,843 controls.

The effect Each copy of the T allele carried 0.39 times the odds of Early-onset myasthenia gravis (95% confidence interval 0.3-0.48); p = 3 × 10−91.

How common The T allele had a frequency of about 91% in the people studied.

Where it sits Chromosome 6, band 6p21.33 — between genes, 0.8 kb from RNU6-283P.

What each result means

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

Questions about rs2853986

What is rs2853986?

rs2853986 is a single position in the genome, in or near the near RNU6-283P gene. Published research associates it with early-onset myasthenia gravis. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs2853986 linked to?

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

Does having rs2853986 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 rs2853986 come from?

GWAS Catalog, Nature communications 2024, PMID:39537604. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.

Quoting this page

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Early-onset myasthenia gravis (rs2853986). MyGeneLog™. https://www.mygenelog.com/variants/rs2853986

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