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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 6,258 Finnish ancestry individuals.
The effect
Each copy of the T allele shifted the measure 0.151 higher (95% confidence interval 0.11-0.19); p = 4 × 10−13.
How common The T allele had a frequency of about 25% in the people studied.
Where it sits Chromosome 1, band 1p34.2 — between genes, 7.2 kb from Y_RNA.
What each result means
G/GNo copy of the version the research linked to Phosphatidylethanolamine (18:0_0:0) levels. This is the starting point the study compared everyone against.
G/TOne copy of the version the research linked to Phosphatidylethanolamine (18:0_0:0) levels. That is a smaller link than two copies.
T/TTwo copies of the version the research linked to Phosphatidylethanolamine (18:0_0:0) levels. That is the strongest link of the three results. A link in a study is not a diagnosis.
Nature communications · 2023 · PMID 37907536 · open access
Questions about rs7529794
What is rs7529794?
rs7529794 is a single position in the genome, in or near the near Y_RNA gene. Published research associates it with phosphatidylethanolamine (18:0_0:0) levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs7529794 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 rs7529794 come from?
GWAS Catalog, Nature communications 2023, PMID:37907536. 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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