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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 282,271 European ancestry individuals.
The effect
The reported allele is C; the catalogue records no effect size
; p = 2 × 10−10.
How common The C allele had a frequency of about 82% in the people studied.
Where it sits Chromosome 17, band 17q21.31 — in an intron of PLEKHM1.
What each result means
C/CTwo copies of the version the research linked to Dietary macronutrient intake (multi-trait analysis). That is the strongest link of the three results. A link in a study is not a diagnosis.
C/GOne copy of the version the research linked to Dietary macronutrient intake (multi-trait analysis). That is a smaller link than two copies.
G/GNo copy of the version the research linked to Dietary macronutrient intake (multi-trait analysis). This is the starting point the study compared everyone against.
rs1971631 is a single position in the genome, in or near the PLEKHM1 gene. Published research associates it with dietary macronutrient intake (multi-trait analysis). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs1971631 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 rs1971631 come from?
GWAS Catalog, Nature human behaviour 2022, PMID:34426670. 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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