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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 37,589 British ancestry individuals.
The effect
Each copy of the G allele shifted the measure 0.05 higher (95% confidence interval 0.03-0.07); p = 1 × 10−10.
How common The G allele had a frequency of about 42% in the people studied.
Where it sits Chromosome 12, band 12p13.32 — in an intron of LINC03141.
What each result means
A/ANo copy of the version the research linked to Pancreas proton density fat fraction. This is the starting point the study compared everyone against.
A/GOne copy of the version the research linked to Pancreas proton density fat fraction. That is a smaller link than two copies.
G/GTwo copies of the version the research linked to Pancreas proton density fat fraction. That is the strongest link of the three results. A link in a study is not a diagnosis.
Journal of obesity · 2025 · PMID 40922984 · open access
Questions about rs7138126
What is rs7138126?
rs7138126 is a single position in the genome, in or near the LINC03141 gene. Published research associates it with pancreas proton density fat fraction. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs7138126 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 rs7138126 come from?
GWAS Catalog, Journal of obesity 2025, PMID:40922984. 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
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Pancreas proton density fat fraction (rs7138126). MyGeneLog™. https://www.mygenelog.com/variants/rs7138126