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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 154,673 European ancestry individuals.
The effect
Each copy of the A allele shifted the measure 0.0279 lower (95% confidence interval 0.019-0.037); p = 4 × 10−10.
How common The A allele had a frequency of about 21% in the people studied.
Where it sits Chromosome 4, band 4q31.3 — in an intron of LINC03074.
What each result means
A/ATwo copies of the version the research linked to Salami liking. That is the strongest link of the three results. A link in a study is not a diagnosis.
A/COne copy of the version the research linked to Salami liking. That is a smaller link than two copies.
C/CNo copy of the version the research linked to Salami liking. This is the starting point the study compared everyone against.
Nature communications · 2022 · PMID 35585065 · open access
Questions about rs1385782
What is rs1385782?
rs1385782 is a single position in the genome, in or near the LINC03074 gene. Published research associates it with salami liking. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs1385782 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 rs1385782 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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