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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 562,259 European ancestry individuals.
The effect
Each copy of the C allele shifted the measure 0.0133 SD unit lower (95% confidence interval 0.0092-0.0174); p = 2 × 10−10.
How common The C allele had a frequency of about 27% in the people studied.
Where it sits Chromosome 15, band 15q21.3 — in an intron of CGNL1.
What each result means
C/CTwo copies of the version the research linked to Hematocrit. That is the strongest link of the three results. A link in a study is not a diagnosis.
C/GOne copy of the version the research linked to Hematocrit. That is a smaller link than two copies.
G/GNo copy of the version the research linked to Hematocrit. This is the starting point the study compared everyone against.
rs8034838 is a single position in the genome, in or near the CGNL1 gene. Published research associates it with hematocrit. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs8034838 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 rs8034838 come from?
GWAS Catalog, Cell 2020, PMID:32888493. 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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