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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 3,273 European ancestry female cases, 24,009 European ancestry female controls.
The effect
Each copy of the G allele shifted the measure 0.352 lower (95% confidence interval 0.27-0.44); p = 2 × 10−16.
How common The G allele had a frequency of about 15% in the people studied.
Where it sits Chromosome 11, band 11p14.1 — in an intron of ARL14EP-DT.
What each result means
A/ANo copy of the version the research linked to Spontaneous dizygotic twinning. This is the starting point the study compared everyone against.
A/GOne copy of the version the research linked to Spontaneous dizygotic twinning. That is a smaller link than two copies.
G/GTwo copies of the version the research linked to Spontaneous dizygotic twinning. That is the strongest link of the three results. A link in a study is not a diagnosis.
Twin research and human genetics : the official journal of the International Society for Twin Studies · 2023 · PMID 37994447
Questions about rs75525300
What is rs75525300?
rs75525300 is a single position in the genome, in or near the ARL14EP-DT gene. Published research associates it with spontaneous dizygotic twinning. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs75525300 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 rs75525300 come from?
GWAS Catalog, Twin research and human genetics : the official journal of the International Society for Twin Studies 2023, PMID:37994447. 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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