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X-18922 levels

near CYP4A11 · rs11585982

What the study found

Who was studied 6,136 Finnish ancestry individuals.

The effect Each copy of the C allele shifted the measure 0.16 lower; p = 9 × 10−13.

Where it sits Chromosome 1, band 1p33 — between genes, 1.8 kb from CYP4A11.

What each result means

C/C Two copies of the version the research linked to X-18922 levels. That is the strongest link of the three results. A link in a study is not a diagnosis.
C/T One copy of the version the research linked to X-18922 levels. That is a smaller link than two copies.
T/T No copy of the version the research linked to X-18922 levels. This is the starting point the study compared everyone against.
Source

Questions about rs11585982

What is rs11585982?

rs11585982 is a single position in the genome, in or near the near CYP4A11 gene. Published research associates it with x-18922 levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs11585982 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 rs11585982 come from?

GWAS Catalog, Nature communications 2022, PMID:35347128. 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.

X-18922 levels (rs11585982). MyGeneLog™. https://www.mygenelog.com/variants/rs11585982

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