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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 A; the catalogue records no effect size
; p = 9 × 10−14.
How common The A allele had a frequency of about 41% in the people studied.
Where it sits Chromosome 15, band 15q14 — between genes, 101.8 kb from LINC02853.
What each result means
A/ATwo copies of the version the research linked to Facial morphology (segment 31). 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 Facial morphology (segment 31). That is a smaller link than two copies.
G/GNo copy of the version the research linked to Facial morphology (segment 31). This is the starting point the study compared everyone against.
Nature genetics · 2021 · PMID 33288918 · open access
Questions about rs34961041
What is rs34961041?
rs34961041 is a single position in the genome, in or near the near LINC02853 gene. Published research associates it with facial morphology (segment 31). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs34961041 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 rs34961041 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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