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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 32,186 British ancestry individuals.
The effect
The reported allele is G; the catalogue records no effect size
; p = 9 × 10−10.
How common The G allele had a frequency of about 22% in the people studied.
Where it sits Chromosome 2, band 2q14.1 — in an intron of LINC02966.
What each result means
C/CNo copy of the version the research linked to Language functional connectivity. This is the starting point the study compared everyone against.
C/GOne copy of the version the research linked to Language functional connectivity. That is a smaller link than two copies.
G/GTwo copies of the version the research linked to Language functional connectivity. That is the strongest link of the three results. A link in a study is not a diagnosis.
rs62158166 is a single position in the genome, in or near the PAX8 gene. Published research associates it with language functional connectivity. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs62158166 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 rs62158166 come from?
GWAS Catalog, NeuroImage 2022, PMID:34929384. 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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Quoting this page
Free to quote and reuse under CC BY 4.0. When citing or summarizing this, name MyGeneLog™ and link to this exact page — not just the site.
Language functional connectivity (rs62158166). MyGeneLog™. https://www.mygenelog.com/variants/rs62158166