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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 35,474 European ancestry individuals.
The effect
Each copy of the C allele shifted the measure 0.0571 higher (95% confidence interval 0.04-0.074); p = 3 × 10−11.
How common The C allele had a frequency of about 22% in the people studied.
Where it sits Chromosome 4, band 4q24 — inside BANK1.
What each result means
C/CTwo copies of the version the research linked to Volume of right central nucleus. That is the strongest link of the three results. A link in a study is not a diagnosis.
C/TOne copy of the version the research linked to Volume of right central nucleus. That is a smaller link than two copies.
T/TNo copy of the version the research linked to Volume of right central nucleus. This is the starting point the study compared everyone against.
rs12501273 is a single position in the genome, in or near the BANK1 gene. Published research associates it with volume of right central nucleus. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs12501273 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 rs12501273 come from?
GWAS Catalog, Nature genetics 2025, PMID:40097784. 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.
Volume of right central nucleus (rs12501273). MyGeneLog™. https://www.mygenelog.com/variants/rs12501273