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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 68,732 European ancestry individuals; replicated in 8,643 European ancestry individuals.
The effect
Each copy of the C allele shifted the measure 6.51 z-score higher; p = 7 × 10−11.
Where it sits Chromosome 1, band 1q42.13 — in an intron of WNT3A.
What each result means
C/CTwo copies of the version the research linked to Gestational duration. That is the strongest link of the three results. A link in a study is not a diagnosis.
C/GOne copy of the version the research linked to Gestational duration. That is a smaller link than two copies.
G/GNo copy of the version the research linked to Gestational duration. This is the starting point the study compared everyone against.
PLoS genetics · 2023 · PMID 37871108 · open access
Questions about rs708119
What is rs708119?
rs708119 is a single position in the genome, in or near the WNT3A gene. Published research associates it with gestational duration. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs708119 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 rs708119 come from?
GWAS Catalog, PLoS genetics 2023, PMID:37871108. 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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