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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 684,122 European ancestry individuals.
The effect
Each copy of the T allele shifted the measure 0.023 lower; p = 4 × 10−11.
Where it sits Chromosome 9, band 9q32 — a missense change in RGS3.
What each result means
C/CPublished research associates this genotype with typical/baseline likelihood of Hemoglobin levels — no copies of the reported risk allele.
C/TPublished research associates this genotype (one copy of the reported risk allele) with an intermediate association with Hemoglobin levels.
T/TPublished research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Hemoglobin levels compared to the general population.
Communications biology · 2020 · PMID 32327693 · open access
Questions about rs113797410
What is rs113797410?
rs113797410 is a single position in the genome, in or near the RGS3 gene. Published research associates it with hemoglobin levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs113797410 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 rs113797410 come from?
GWAS Catalog, Communications biology 2020, PMID:32327693. 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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