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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 125,000 African ancestry individuals (MTAG boosted by total cholesterol and triglyceride samples).
The effect
Each copy of the G allele shifted the measure 0.027 lower (95% confidence interval 0.019-0.035); p = 3 × 10−12.
Where it sits Chromosome 9, band 9q31.2 — between genes, 43.3 kb from RNU6-996P.
What each result means
G/GTwo copies of the version the research linked to High-density lipoprotein levels (MTAG). 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 High-density lipoprotein levels (MTAG). That is a smaller link than two copies.
T/TNo copy of the version the research linked to High-density lipoprotein levels (MTAG). This is the starting point the study compared everyone against.
Nature communications · 2023 · PMID 37669986 · open access
Questions about rs2017419
What is rs2017419?
rs2017419 is a single position in the genome, in or near the near RNU6-996P gene. Published research associates it with high-density lipoprotein levels (mtag). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs2017419 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 rs2017419 come from?
GWAS Catalog, Nature communications 2023, PMID:37669986. 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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