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Stands on its own.
Nothing else here links to this position yet — but the page above is the point: what the
research found, what each genotype means, and where it came from, in language you can
read. Links to conditions, drugs and the senses appear automatically if we write them.
What the study found
Who was studied 1,383 Danish ancestry cases, 62,656 Danish ancestry controls.
The effect
Each copy of the A allele carried 1.83 times the odds of Autoimmune traits (95% confidence interval 1.6-2.1); p = 2 × 10−15.
How common The A allele had a frequency of about 5% in the people studied.
Where it sits Chromosome 6, band 6p21.33 — a missense change in EHMT2.
What each result means
A/ATwo copies of the version the research linked to Autoimmune traits. That is the strongest link of the three results. A link in a study is not a diagnosis.
A/GOne copy of the version the research linked to Autoimmune traits. That is a smaller link than two copies.
G/GNo copy of the version the research linked to Autoimmune traits. This is the starting point the study compared everyone against.
Brain, behavior, and immunity · 2021 · PMID 32534018
Questions about rs115884658
What is rs115884658?
rs115884658 is a single position in the genome, in or near the EHMT2 gene. Published research associates it with autoimmune traits. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs115884658 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 rs115884658 come from?
GWAS Catalog, Brain, behavior, and immunity 2021, PMID:32534018. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
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