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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 408,112 British individuals.
The effect
Each copy of the C allele shifted the measure 0.0635 lower (95% confidence interval 0.052-0.075); p = 9 × 10−28.
How common The C allele had a frequency of about 4% in the people studied.
Where it sits Chromosome 7, band 7q22.1 — in an intron of ARPC1B.
What each result means
C/CTwo copies of the version the research linked to Reticulocyte count. 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 Reticulocyte count. That is a smaller link than two copies.
T/TNo copy of the version the research linked to Reticulocyte count. This is the starting point the study compared everyone against.
rs117370443 is a single position in the genome, in or near the ARPC1B gene. Published research associates it with reticulocyte count. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs117370443 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 rs117370443 come from?
GWAS Catalog, Cell 2020, PMID:32888494. 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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