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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 2,466 Black/admixed ancestry individuals; replicated in up to 1,653 European, Hispanic, Asian or Black individuals.
The effect
Each copy of the G allele shifted the measure 0.228 lower (95% confidence interval 0.16-0.29); p = 5 × 10−12.
Where it sits Chromosome 10, band 10q25.2 — in an intron of GPAM.
What each result means
G/GTwo copies of the version the research linked to N6-methyllysine levels. That is the strongest link of the three results. A link in a study is not a diagnosis.
G/TOne copy of the version the research linked to N6-methyllysine levels. That is a smaller link than two copies.
T/TNo copy of the version the research linked to N6-methyllysine levels. This is the starting point the study compared everyone against.
Nature communications · 2022 · PMID 35995766 · open access
Questions about rs7079286
What is rs7079286?
rs7079286 is a single position in the genome, in or near the GPAM gene. Published research associates it with n6-methyllysine levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs7079286 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 rs7079286 come from?
GWAS Catalog, Nature communications 2022, PMID:35995766. 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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