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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 13,493 European ancestry individuals.
The effect
Each copy of the A allele shifted the measure 0.439 higher (95% confidence interval 0.33-0.55); p = 2 × 10−15.
How common The A allele had a frequency of about 42% in the people studied.
Where it sits Chromosome 6, band 6p22.3 — between genes, 16 kb from NHLRC1.
What each result means
A/ATwo copies of the version the research linked to Intrinsic epigenetic age acceleration. That is the strongest link of the three results. A link in a study is not a diagnosis.
A/TOne copy of the version the research linked to Intrinsic epigenetic age acceleration. That is a smaller link than two copies.
T/TNo copy of the version the research linked to Intrinsic epigenetic age acceleration. This is the starting point the study compared everyone against.
PLoS genetics · 2019 · PMID 31738745 · open access
Questions about rs7744541
What is rs7744541?
rs7744541 is a single position in the genome, in or near the near NHLRC1 gene. Published research associates it with intrinsic epigenetic age acceleration. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs7744541 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 rs7744541 come from?
GWAS Catalog, PLoS genetics 2019, PMID:31738745. 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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Quoting this page
Free to quote and reuse under CC BY 4.0. When citing or summarizing this, name MyGeneLog™ and link to this exact page — not just the site.
Intrinsic epigenetic age acceleration (rs7744541). MyGeneLog™. https://www.mygenelog.com/variants/rs7744541