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Who was studied 405,540 European ancestry individuals.
The effect
Each copy of the C allele shifted the measure 0.0102 higher (95% confidence interval 0.0068-0.0136); p = 5 × 10−9.
How common The C allele had a frequency of about 84% in the people studied.
Where it sits Chromosome 3, band 3q29 — in an intron of XXYLT1.
What each result means
C/CTwo copies of the version the research linked to Height (baseline). That is the strongest link of the three results. A link in a study is not a diagnosis.
C/TOne copy of the version the research linked to Height (baseline). That is a smaller link than two copies.
T/TNo copy of the version the research linked to Height (baseline). This is the starting point the study compared everyone against.
Nature communications · 2025 · PMID 40374629 · open access
Questions about rs73206626
What is rs73206626?
rs73206626 is a single position in the genome, in or near the XXYLT1 gene. Published research associates it with height (baseline). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
What conditions is rs73206626 linked to?
On MyGeneLog this position is linked to Height. The research behind each link, and its sources, are set out on that condition page.
Does having rs73206626 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 rs73206626 come from?
GWAS Catalog, Nature communications 2025, PMID:40374629. 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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