Bone mineral density (paediatric, total body less head)
FAM3C · rs7776725
11 452235222225Reads by AI crawlersClaude2ChatGPT2Google · Gemini0Perplexity3Meta AI5Microsoft · Copilot2Amazon2Apple2China (ByteDance, Huawei, Baidu…)2ByteDance (Doubao)2Others25Total45Counted 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.
Solid lines are connections this site curates. Dashed lines mean the two ends share a research paper — worth knowing, and not a claim that one explains the other.
What the study found
Who was studied 8,007 European ancestry children, 289 Surinamese ancestry children, 300 Turkish ancestry children, 232 Moroccan ancestry children, 588 children.
The effect
Each copy of the C allele shifted the measure 0.158 higher (95% confidence interval 0.12-0.2); p = 2 × 10−15.
Where it sits Chromosome 7, band 7q31.31 — in an intron of FAM3C.
What each result means
C/CTwo copies of the version the research linked to Bone mineral density (paediatric, total body less head). 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 Bone mineral density (paediatric, total body less head). That is a smaller link than two copies.
T/TNo copy of the version the research linked to Bone mineral density (paediatric, total body less head). This is the starting point the study compared everyone against.
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 rs7776725
What is rs7776725?
rs7776725 is a single position in the genome, in or near the FAM3C gene. Published research associates it with bone mineral density (paediatric, total body less head). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
What conditions is rs7776725 linked to?
On MyGeneLog this position is linked to Paediatric Bone Mineral Density. The research behind each link, and its sources, are set out on that condition page.
What do people read about alongside rs7776725?
Subjects that appear in the title or abstract of the same papers as this rsID include bones and fractures (9 papers). A shared paper means somebody wrote about the two together; it is not a claim that this position explains the topic.
Does having rs7776725 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 rs7776725 come from?
GWAS Catalog, PLoS Genet 2014, PMID:24945404. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
11 452235222225Reads by AI crawlersClaude2ChatGPT2Google · Gemini0Perplexity3Meta AI5Microsoft · Copilot2Amazon2Apple2China (ByteDance, Huawei, Baidu…)2ByteDance (Doubao)2Others25Total45Counted 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.
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Bone mineral density (paediatric, total body less head) (rs7776725). MyGeneLog™. https://www.mygenelog.com/variants/rs7776725