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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 4,680 European ancestry individuals; replicated in 3,566 European ancestry individuals.
The effect
The reported allele is G; the catalogue records no effect size
; p = 4 × 10−11.
How common The G allele had a frequency of about 20% in the people studied.
Where it sits Chromosome 4, band 4q28.1 — between genes, 49.8 kb from LINC02379.
What each result means
A/ANo copy of the version the research linked to Facial morphology (segment 24). This is the starting point the study compared everyone against.
A/GOne copy of the version the research linked to Facial morphology (segment 24). That is a smaller link than two copies.
G/GTwo copies of the version the research linked to Facial morphology (segment 24). That is the strongest link of the three results. A link in a study is not a diagnosis.
Nature genetics · 2021 · PMID 33288918 · open access
Questions about rs6852838
What is rs6852838?
rs6852838 is a single position in the genome, in or near the near LINC02379 gene. Published research associates it with facial morphology (segment 24). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs6852838 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 rs6852838 come from?
GWAS Catalog, Nature genetics 2021, PMID:33288918. 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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