ADAMTS5 · rs2830585
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 997 European ancestry individuals; replicated in 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals.
The effect Each copy of the T allele shifted the measure 1.07 lower (95% confidence interval 0.99-1.16); p = 4 × 10−104.
Where it sits Chromosome 21, band 21q21.3 — a missense change in ADAMTS5.
What ClinVar records
Classification
Benign; criteria provided, multiple submitters, no conflicts (2 of 4 stars, 2 submitters), last evaluated 2020-07-15.
ClinVar record 1181193 NM_007038.5(ADAMTS5):c.1841G>A (p.Arg614His)
What this is ClinVar's aggregate record for this position (as of its 2026-10-12 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.
rs2830585 is a single position in the genome, in or near the ADAMTS5 gene. Published research associates it with a disintegrin and metalloproteinase with thrombospondin motifs 5 levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
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.
GWAS Catalog, Nature communications 2017, PMID:28240269. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
Free to quote and reuse under CC BY 4.0. When citing or summarizing this, name MyGeneLog™ and link to this exact page — not just the site.
A disintegrin and metalloproteinase with thrombospondin motifs 5 levels (rs2830585). MyGeneLog™. https://www.mygenelog.com/variants/rs2830585