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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 1,237 Southern Han Chinese ancestry individuals; replicated in 4,093 East Asian ancestry individuals.
The effect
Each copy of the G allele shifted the measure 0.36 lower; p = 8 × 10−11.
Where it sits Chromosome 4, band 4q35.1 — in an intron of TENM3.
What each result means
G/GTwo copies of the version the research linked to Spherical equivalent. That is the strongest link of the three results. A link in a study is not a diagnosis.
G/TOne copy of the version the research linked to Spherical equivalent. That is a smaller link than two copies.
T/TNo copy of the version the research linked to Spherical equivalent. This is the starting point the study compared everyone against.
NPJ genomic medicine · 2025 · PMID 40410244 · open access
Questions about rs17074027
What is rs17074027?
rs17074027 is a single position in the genome, in or near the TENM3 gene. Published research associates it with spherical equivalent. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs17074027 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 rs17074027 come from?
GWAS Catalog, NPJ genomic medicine 2025, PMID:40410244. 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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