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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 2,483 East Asian ancestry individuals, 1,885 European ancestry individuals, 11,146 individuals; replicated in 10,074 European ancestry individuals, 2,870 European and other ancestry individuals, 21,434 individuals.
The effect
Each copy of the G allele shifted the measure 0.06 higher (95% confidence interval 0.04-0.08); p = 4 × 10−12.
How common The G allele had a frequency of about 35% in the people studied.
Where it sits Chromosome 19, band 19q13.11 — a missense change in GPATCH1.
What each result means
A/ANo copy of the version the research linked to Bone properties (heel). This is the starting point the study compared everyone against.
A/GOne copy of the version the research linked to Bone properties (heel). That is a smaller link than two copies.
G/GTwo copies of the version the research linked to Bone properties (heel). That is the strongest link of the three results. A link in a study is not a diagnosis.
Papers in Europe PMC whose title or abstract names both this rsID and that subject. A shared paper means somebody wrote about the two together — it is not a claim that this position explains the subject.
Questions about rs10416265
What is rs10416265?
rs10416265 is a single position in the genome, in or near the GPATCH1 gene. Published research associates it with bone properties (heel). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
What do people read about alongside rs10416265?
Subjects that appear in the title or abstract of the same papers as this rsID include bones and fractures (2 papers). A shared paper means somebody wrote about the two together; it is not a claim that this position explains the topic.
Does having rs10416265 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 rs10416265 come from?
GWAS Catalog, Hum Mol Genet 2014, PMID:24430505. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
3 442215122227Reads by AI crawlersClaude2ChatGPT2Google · Gemini0Perplexity1Meta AI5Microsoft · Copilot1Amazon2Apple2China (ByteDance, Huawei, Baidu…)2ByteDance (Doubao)2Others27Total44Counted by the name each crawler declares; requests found to be impersonating one are left out. Google · Gemini includes Googlebot, the search crawler whose index Google also uses for its AI features. Other search engines and bots are under Others.
Quoting this page
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.
Bone properties (heel) (rs10416265). MyGeneLog™. https://www.mygenelog.com/variants/rs10416265