0 1518222Reads by AI crawlersClaude0ChatGPT0Google · Gemini0Perplexity1Meta AI0Microsoft · Copilot8Amazon2Apple0China (ByteDance, Huawei, Baidu…)2ByteDance (Doubao)2Others2Total15Counted 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.
Who was studied 16,204 European ancestry individuals.
The effect
Each copy of the A allele shifted the measure 3.36 μm higher (95% confidence interval 2.51-4.2); p = 8 × 10−15.
How common The A allele had a frequency of about 48% in the people studied.
Where it sits Chromosome 9, band 9q34.3 — between genes, 3.6 kb from LINC02692.
What each result means
A/ATwo copies of the version the research linked to Central corneal thickness. That is the strongest link of the three results. A link in a study is not a diagnosis.
A/GOne copy of the version the research linked to Central corneal thickness. That is a smaller link than two copies.
G/GNo copy of the version the research linked to Central corneal thickness. This is the starting point the study compared everyone against.
Communications biology · 2019 · PMID 31798171 · open access
Questions about rs7868669
What is rs7868669?
rs7868669 is a single position in the genome, in or near the LCN12 gene. Published research associates it with central corneal thickness. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
What conditions is rs7868669 linked to?
On MyGeneLog this position is linked to Central Corneal Thickness. The research behind each link, and its sources, are set out on that condition page.
Does having rs7868669 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 rs7868669 come from?
GWAS Catalog, Communications biology 2019, PMID:31798171. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
0 1518222Reads by AI crawlersClaude0ChatGPT0Google · Gemini0Perplexity1Meta AI0Microsoft · Copilot8Amazon2Apple0China (ByteDance, Huawei, Baidu…)2ByteDance (Doubao)2Others2Total15Counted 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.
Central corneal thickness (rs7868669). MyGeneLog™. https://www.mygenelog.com/variants/rs7868669