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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 164,818 European ancestry individuals.
The effect
Each copy of the A allele shifted the measure 0.03 higher (95% confidence interval 0.022-0.038); p = 3 × 10−16.
Where it sits Chromosome 1, band 1p32.3 — between genes, 12.3 kb from CDKN2C.
What each result means
A/ATwo copies of the version the research linked to Thyroid stimulating hormone levels. 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 Thyroid stimulating hormone levels. That is a smaller link than two copies.
G/GNo copy of the version the research linked to Thyroid stimulating hormone levels. This is the starting point the study compared everyone against.
European journal of endocrinology · 2024 · PMID 39067062
Questions about rs12567744
What is rs12567744?
rs12567744 is a single position in the genome, in or near the near CDKN2C gene. Published research associates it with thyroid stimulating hormone levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs12567744 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 rs12567744 come from?
GWAS Catalog, European journal of endocrinology 2024, PMID:39067062. 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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