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F-caffeinated/sweet liking (derived food-liking factor)

PRH1 · rs61912249

What the study found

Who was studied 155,986 European ancestry individuals.

The effect Each copy of the T allele shifted the measure 0.102 lower (95% confidence interval 0.072-0.133); p = 3 × 10−11.

How common The T allele had a frequency of about 25% in the people studied.

Where it sits Chromosome 12, band 12p13.2 — in an intron of PRH1.

What each result means

A/A No copy of the version the research linked to F-caffeinated/sweet liking (derived food-liking factor). This is the starting point the study compared everyone against.
A/T One copy of the version the research linked to F-caffeinated/sweet liking (derived food-liking factor). That is a smaller link than two copies.
T/T Two copies of the version the research linked to F-caffeinated/sweet liking (derived food-liking factor). That is the strongest link of the three results. A link in a study is not a diagnosis.
Source

Questions about rs61912249

What is rs61912249?

rs61912249 is a single position in the genome, in or near the PRH1 gene. Published research associates it with f-caffeinated/sweet 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 rs61912249 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 rs61912249 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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F-caffeinated/sweet liking (derived food-liking factor) (rs61912249). MyGeneLog™. https://www.mygenelog.com/variants/rs61912249

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