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Who was studied 295,529 European ancestry individuals, 8,231 Latino individuals, 3,058 African American individuals, 2,029 African British individuals, 7,701 East Asian ancestry individuals, 2,735 South Asian ancestry individuals, 1,979 mixed and unknown ancestry individuals.
The effect
Each copy of the T allele shifted the measure 0.154 lower; p = 3 × 10−10.
Where it sits Chromosome 19, band 19q12 — between genes, 6.3 kb from CCNE1.
What each result means
G/GNo copy of the version the research linked to Diastolic blood pressure. This is the starting point the study compared everyone against.
G/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.
Nature genetics · 2017 · PMID 27841878 · open access
Questions about rs34331990
What is rs34331990?
rs34331990 is a single position in the genome, in or near the CCNE1 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 rs34331990 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 rs34331990 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 rs34331990 come from?
GWAS Catalog, Nature genetics 2017, PMID:27841878. 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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