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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 159,393 European ancestry individuals.
The effect
Each copy of the C allele shifted the measure 0.0973 higher (95% confidence interval 0.072-0.123); p = 7 × 10−14.
How common The C allele had a frequency of about 40% in the people studied.
Where it sits Chromosome 16, band 16p11.2 — in the 3′ untranslated region of TUFM.
What each result means
A/ANo copy of the version the research linked to Milky sweets liking. This is the starting point the study compared everyone against.
A/COne copy of the version the research linked to Milky sweets liking. That is a smaller link than two copies.
C/CTwo copies of the version the research linked to Milky sweets liking. 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 rs3088215
What is rs3088215?
rs3088215 is a single position in the genome, in or near the TUFM gene. Published research associates it with milky sweets liking. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs3088215 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 rs3088215 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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