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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 325,027 European ancestry individuals.
The effect
Each copy of the A allele shifted the measure 0.023 lower (95% confidence interval 0.019-0.027); p = 6 × 10−29.
Where it sits Chromosome 10, band 10q22.3 — in an intron of LRMDA.
What each result means
A/ATwo copies of the version the research linked to Chronic obstructive pulmonary disease liability (machine learning-based score). That is the strongest link of the three results. A link in a study is not a diagnosis.
A/GOne copy of the version the research linked to Chronic obstructive pulmonary disease liability (machine learning-based score). That is a smaller link than two copies.
G/GNo copy of the version the research linked to Chronic obstructive pulmonary disease liability (machine learning-based score). This is the starting point the study compared everyone against.
rs2256413 is a single position in the genome, in or near the LRMDA gene. Published research associates it with chronic obstructive pulmonary disease liability (machine learning-based score). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs2256413 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 rs2256413 come from?
GWAS Catalog, Nature genetics 2023, PMID:37069358. 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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