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Who was studied 253,288 European ancestry individuals; replicated in 80,067 European ancestry individuals.
The effect
Each copy of the T allele shifted the measure 0.029 higher (95% confidence interval 0.023-0.035); p = 6 × 10−20.
How common The T allele had a frequency of about 67% in the people studied.
Where it sits Chromosome 15, band 15q26.3 — in the 3′ untranslated region of ADAMTS17.
What ClinVar records
ClassificationBenign for Weill-Marchesani 4 syndrome, recessive, Sarcoma, Cervical cancer, Lung cancer; criteria provided, multiple submitters, no conflicts (2 of 4 stars, 3 submitters), last evaluated 2018-01-13.
ClinVar record 315184NM_139057.4(ADAMTS17):c.*1449G>A
What this is ClinVar's aggregate record for this position (as of its 2026-10-19 release), not a result about you. A classification describes the variant against the condition named, as laboratories submitted it. Whether a person carries this variant, and what that would mean for them, is a question for a clinical test and a genetic counsellor.
What each result means
C/CNo copy of the version the research linked to Height. This is the starting point the study compared everyone against.
C/TOne copy of the version the research linked to Height. That is a smaller link than two copies.
T/TTwo copies of the version the research linked to Height. That is the strongest link of the three results. A link in a study is not a diagnosis.
Nature genetics · 2014 · PMID 25282103 · open access
Questions about rs2573625
What is rs2573625?
rs2573625 is a single position in the genome, in or near the ADAMTS17 gene. Published research associates it with height. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
What conditions is rs2573625 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 rs2573625 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 rs2573625 come from?
GWAS Catalog, Nature genetics 2014, PMID:25282103. 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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