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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 2,908 European ancestry cases, 436,579 European ancestry controls; replicated in 1,485 European ancestry cases, 137,185 European ancestry controls.
The effect
Each copy of the G allele shifted the measure 6.29 z score higher; p = 3 × 10−10.
Where it sits Chromosome 11, band 11q13.1 — in an intron of LTBP3.
What each result means
A/ANo copy of the version the research linked to Trigger finger. This is the starting point the study compared everyone against.
A/GOne copy of the version the research linked to Trigger finger. That is a smaller link than two copies.
G/GTwo copies of the version the research linked to Trigger finger. That is the strongest link of the three results. A link in a study is not a diagnosis.
The Lancet. Rheumatology · 2022 · PMID 36043126 · open access
Questions about rs4244811
What is rs4244811?
rs4244811 is a single position in the genome, in or near the LTBP3 gene. Published research associates it with trigger finger. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs4244811 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 rs4244811 come from?
GWAS Catalog, The Lancet. Rheumatology 2022, PMID:36043126. 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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