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Who was studied 73,265 European ancestry individuals.
The effect
Each copy of the T allele shifted the measure 0.193 higher (95% confidence interval 0.14-0.25); p = 2 × 10−11.
Where it sits Chromosome 6, band 6p21.33 — in an intron of LSM2.
What each result means
A/ANo copy of the version the research linked to Rosacea symptom severity. This is the starting point the study compared everyone against.
A/TOne copy of the version the research linked to Rosacea symptom severity. That is a smaller link than two copies.
T/TTwo copies of the version the research linked to Rosacea symptom severity. That is the strongest link of the three results. A link in a study is not a diagnosis.
Human molecular genetics · 2018 · PMID 29771307 · open access
Questions about rs1144710
What is rs1144710?
rs1144710 is a single position in the genome, in or near the LSM2 gene. Published research associates it with rosacea symptom severity. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
What conditions is rs1144710 linked to?
On MyGeneLog this position is linked to Rosacea. The research behind each link, and its sources, are set out on that condition page.
Does having rs1144710 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 rs1144710 come from?
GWAS Catalog, Hum Mol Genet 2018, PMID:29771307. 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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