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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 2,961 Han Chinese ancestry individuals, 721 Uyghur ancestry individuals, 2,301 Latin American ancestry individuals; replicated in 4,411 Dutch ancestry individuals.
The effect
The reported allele is A; the catalogue records no effect size
; p = 6 × 10−11.
Where it sits Chromosome 2, band 2q12.3 — in an intron of LIMS1.
What each result means
A/ATwo copies of the version the research linked to Eyebrow thickness. 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 Eyebrow thickness. That is a smaller link than two copies.
G/GNo copy of the version the research linked to Eyebrow thickness. This is the starting point the study compared everyone against.
PLoS genetics · 2018 · PMID 30248107 · open access
Questions about rs1866188
What is rs1866188?
rs1866188 is a single position in the genome, in or near the EDAR gene. Published research associates it with eyebrow thickness. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs1866188 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 rs1866188 come from?
GWAS Catalog, PLoS Genet 2018, PMID:30248107. 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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