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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 14,739 African American individuals, 6,762 African ancestry individuals, 21,686 Hispanic/Latino individuals; replicated in 7,037 African American individuals.
The effect
Each copy of the T allele shifted the measure 0.076 lower; p = 7 × 10−13.
Where it sits Chromosome 16, band 16p13.3 — in an intron of NPRL3.
What each result means
C/CNo copy of the version the research linked to Hemoglobin levels. This is the starting point the study compared everyone against.
C/TOne copy of the version the research linked to Hemoglobin levels. That is a smaller link than two copies.
T/TTwo copies of the version the research linked to Hemoglobin levels. That is the strongest link of the three results. A link in a study is not a diagnosis.
PLoS genetics · 2019 · PMID 31869403 · open access
Questions about rs2562181
What is rs2562181?
rs2562181 is a single position in the genome, in or near the NPRL3 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 rs2562181 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 rs2562181 come from?
GWAS Catalog, PLoS genetics 2019, PMID:31869403. 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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