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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 46,685 European ancestry individuals; replicated in 4,765 non-European ancestry individuals.
The effect
Each copy of the C allele shifted the measure 3.14 lower (95% confidence interval 2.32-3.96); p = 7 × 10−14.
How common The C allele had a frequency of about 7% in the people studied.
Where it sits Chromosome 12, band 12q21.2 — in an intron of NAV3.
What each result means
C/CTwo copies of the version the research linked to Corpus callosum genu area. That is the strongest link of the three results. A link in a study is not a diagnosis.
C/GOne copy of the version the research linked to Corpus callosum genu area. That is a smaller link than two copies.
G/GNo copy of the version the research linked to Corpus callosum genu area. This is the starting point the study compared everyone against.
Nature communications · 2025 · PMID 41188267 · open access
Questions about rs10506772
What is rs10506772?
rs10506772 is a single position in the genome, in or near the NAV3 gene. Published research associates it with corpus callosum genu area. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs10506772 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 rs10506772 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.
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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 genu area (rs10506772). MyGeneLog™. https://www.mygenelog.com/variants/rs10506772