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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 3,566 European ancestry individuals; replicated in 4,680 European ancestry individuals.
The effect
The reported allele is A; the catalogue records no effect size
; p = 3 × 10−11.
How common The A allele had a frequency of about 27% in the people studied.
Where it sits Chromosome 2, band 2q31.1 — in an intron of LINC01117.
What each result means
A/ATwo 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.
A/GOne copy of the version the research linked to Facial morphology (segment 24). That is a smaller link than two copies.
G/GNo copy of the version the research linked to Facial morphology (segment 24). This is the starting point the study compared everyone against.
Nature genetics · 2021 · PMID 33288918 · open access
Questions about rs10178696
What is rs10178696?
rs10178696 is a single position in the genome, in or near the LINC01117 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 rs10178696 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 rs10178696 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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