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Who was studied 47,745 European ancestry individuals.
The effect
Each copy of the G allele shifted the measure 0.0823 higher (95% confidence interval 0.071-0.094); p = 2 × 10−54.
How common The G allele had a frequency of about 66% in the people studied.
Where it sits Chromosome 16, band 16q24.2 — in an intron of BANP.
What each result means
A/ANo copy of the version the research linked to PRTG protein levels. This is the starting point the study compared everyone against.
A/GOne copy of the version the research linked to PRTG protein levels. That is a smaller link than two copies.
G/GTwo copies of the version the research linked to PRTG protein levels. That is the strongest link of the three results. A link in a study is not a diagnosis.
Nature genetics · 2025 · PMID 39789286 · open access
Questions about rs4843292
What is rs4843292?
rs4843292 is a single position in the genome, in or near the BANP gene. Published research associates it with prtg protein levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
What conditions is rs4843292 linked to?
On MyGeneLog this position is linked to Celiac Disease. The research behind each link, and its sources, are set out on that condition page.
Does having rs4843292 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 rs4843292 come from?
GWAS Catalog, Nature genetics 2025, PMID:39789286. 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.
PRTG protein levels (rs4843292). MyGeneLog™. https://www.mygenelog.com/variants/rs4843292