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Who was studied 80,950 African ancestry individuals.
The effect
Each copy of the T allele shifted the measure 0.0604 higher (95% confidence interval 0.04-0.081); p = 8 × 10−9.
Where it sits Chromosome 3, band 3p22.2 — in an intron of SLC22A14.
What each result means
C/CNo copy of the version the research linked to Diastolic blood pressure. This is the starting point the study compared everyone against.
C/TOne copy of the version the research linked to Diastolic blood pressure. That is a smaller link than two copies.
T/TTwo copies of the version the research linked to Diastolic blood pressure. That is the strongest link of the three results. A link in a study is not a diagnosis.
International journal of molecular sciences · 2023 · PMID 36768488 · open access
Questions about rs11129785
What is rs11129785?
rs11129785 is a single position in the genome, in or near the SLC22A14 gene. Published research associates it with diastolic blood pressure. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
What conditions is rs11129785 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 rs11129785 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 rs11129785 come from?
GWAS Catalog, International journal of molecular sciences 2023, PMID:36768488. 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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