0 312Reads by AI crawlersClaude0ChatGPT0Google · Gemini0Perplexity0Meta AI0Microsoft · Copilot0Amazon1Apple0China (ByteDance, Huawei, Baidu…)0Others2Total3Counted 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 2,737 British ancestry cases, 47,635 British ancestry controls.
The effect
Each copy of the G allele carried 1.23 times the odds of High myopia (95% confidence interval 1.161475-1.299783); p = 2 × 10−13.
How common The G allele had a frequency of about 36% in the people studied.
Where it sits Chromosome 17, band 17q25.3 — inside PDE6G.
What each result means
A/ANo copy of the version the research linked to High myopia. This is the starting point the study compared everyone against.
A/GOne copy of the version the research linked to High myopia. That is a smaller link than two copies.
G/GTwo copies of the version the research linked to High myopia. That is the strongest link of the three results. A link in a study is not a diagnosis.
Human molecular genetics · 2020 · PMID 31816047 · open access
Questions about rs562698611
What is rs562698611?
rs562698611 is a single position in the genome, in or near the PDE6G gene. Published research associates it with high myopia. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
What conditions is rs562698611 linked to?
On MyGeneLog this position is linked to Myopia. The research behind each link, and its sources, are set out on that condition page.
Does having rs562698611 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 rs562698611 come from?
GWAS Catalog, Human molecular genetics 2020, PMID:31816047. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
0 312Reads by AI crawlersClaude0ChatGPT0Google · Gemini0Perplexity0Meta AI0Microsoft · Copilot0Amazon1Apple0China (ByteDance, Huawei, Baidu…)0Others2Total3Counted 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.
High myopia (rs562698611). MyGeneLog™. https://www.mygenelog.com/variants/rs562698611