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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 158,509 European ancestry individuals.
The effect
Each copy of the T allele shifted the measure 0.0764 lower (95% confidence interval 0.053-0.1); p = 2 × 10−10.
How common The T allele had a frequency of about 50% in the people studied.
Where it sits Chromosome 1, band 1p31.1 — between genes, 13.6 kb from KRT8P21.
What each result means
A/ANo copy of the version the research linked to F-meat liking (derived food-liking factor). This is the starting point the study compared everyone against.
A/TOne copy of the version the research linked to F-meat liking (derived food-liking factor). That is a smaller link than two copies.
T/TTwo copies of the version the research linked to F-meat liking (derived food-liking factor). That is the strongest link of the three results. A link in a study is not a diagnosis.
Nature communications · 2022 · PMID 35585065 · open access
Questions about rs4233100
What is rs4233100?
rs4233100 is a single position in the genome, in or near the near KRT8P21 gene. Published research associates it with f-meat liking (derived food-liking factor). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs4233100 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 rs4233100 come from?
GWAS Catalog, Nature communications 2022, PMID:35585065. 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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