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Who was studied at least 757,601 European ancestry individuals (MTAG boosted by 455,258 Alzheimer's disease samples).
The effect
Each copy of the C allele shifted the measure 0.0174 lower (95% confidence interval 0.012-0.023); p = 5 × 10−10.
Where it sits Chromosome 1, band 1p36.11 — between genes, 1.5 kb from AHDC1.
What each result means
C/CTwo copies of the version the research linked to Systolic blood pressure (MTAG). That is the strongest link of the three results. A link in a study is not a diagnosis.
C/TOne copy of the version the research linked to Systolic blood pressure (MTAG). That is a smaller link than two copies.
T/TNo copy of the version the research linked to Systolic blood pressure (MTAG). This is the starting point the study compared everyone against.
Nature communications · 2024 · PMID 39537608 · open access
Questions about rs17361679
What is rs17361679?
rs17361679 is a single position in the genome, in or near the near AHDC1 gene. Published research associates it with systolic blood pressure (mtag). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
What conditions is rs17361679 linked to?
On MyGeneLog this position is linked to Blood Pressure. The research behind each link, and its sources, are set out on that condition page.
Does having rs17361679 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 rs17361679 come from?
GWAS Catalog, Nature communications 2024, PMID:39537608. 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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