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Corpus callosum anterior body mean thickness

near CABYR · rs113722141

What the study found

Who was studied 46,685 European ancestry individuals; replicated in 4,765 non-European ancestry individuals.

The effect Each copy of the A allele shifted the measure 0.0458 lower (95% confidence interval 0.031-0.06); p = 5 × 10−10.

How common The A allele had a frequency of about 86% in the people studied.

Where it sits Chromosome 18, band 18q11.2 — between genes, 0.6 kb from CABYR.

What each result means

A/A Two copies of the version the research linked to Corpus callosum anterior body mean thickness. That is the strongest link of the three results. A link in a study is not a diagnosis.
A/T One copy of the version the research linked to Corpus callosum anterior body mean thickness. That is a smaller link than two copies.
T/T No copy of the version the research linked to Corpus callosum anterior body mean thickness. This is the starting point the study compared everyone against.
Source

Questions about rs113722141

What is rs113722141?

rs113722141 is a single position in the genome, in or near the near CABYR gene. Published research associates it with corpus callosum anterior body mean thickness. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs113722141 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 rs113722141 come from?

GWAS Catalog, Nature communications 2025, PMID:41188267. 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.

Corpus callosum anterior body mean thickness (rs113722141). MyGeneLog™. https://www.mygenelog.com/variants/rs113722141

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