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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 157,662 European ancestry individuals; replicated in 26,154 European, Central Asian and unknown ancestry individuals.
The effect
Each copy of the C allele shifted the measure 0.0591 lower (95% confidence interval 0.052-0.066); p = 1 × 10−60.
How common The C allele had a frequency of about 52% in the people studied.
Where it sits Chromosome 12, band 12p13.2 — in an intron of PRH1.
What each result means
A/ANo copy of the version the research linked to Grapefruit liking. This is the starting point the study compared everyone against.
A/COne copy of the version the research linked to Grapefruit liking. That is a smaller link than two copies.
C/CTwo copies of the version the research linked to Grapefruit 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 rs61912110
What is rs61912110?
rs61912110 is a single position in the genome, in or near the PRH1 gene. Published research associates it with grapefruit liking. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs61912110 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 rs61912110 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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