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F-sharp flavour liking (derived food-liking factor)

GFRA1 · rs12413585

What the study found

Who was studied 152,547 European ancestry individuals.

The effect Each copy of the A allele shifted the measure 0.064 higher (95% confidence interval 0.047-0.081); p = 7 × 10−13.

How common The A allele had a frequency of about 48% in the people studied.

Where it sits Chromosome 10, band 10q25.3 — in an intron of GFRA1.

What each result means

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

Questions about rs12413585

What is rs12413585?

rs12413585 is a single position in the genome, in or near the GFRA1 gene. Published research associates it with f-sharp flavour 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 rs12413585 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 rs12413585 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.

Quoting this page

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F-sharp flavour liking (derived food-liking factor) (rs12413585). MyGeneLog™. https://www.mygenelog.com/variants/rs12413585

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