0 241218237Reads by AI crawlersClaude1ChatGPT0Google · Gemini2Perplexity1Meta AI8Microsoft · Copilot0Amazon2Apple3China (ByteDance, Huawei, Baidu…)0Others7Total24Counted 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 10,523 European ancestry cases, 203,579 European ancestry controls, 411 Hispanic cases, 4,778 Hispanic controls, 463 East Asian ancestry cases, 4,907 East Asian ancestry controls, 298 African American cases, 1,549 African American controls, 204 South Asian ancestry cases, 4,916 South Asian ancestry controls, 272 African British cases, 4,831 African British controls, 144 mixed ancestry cases, 3,427 mixed ancestry controls.
The effect
Each copy of the G allele carried 1.11 times the odds of Glaucoma (primary open-angle) (95% confidence interval 1.08-1.15); p = 2 × 10−10.
Where it sits Chromosome 6, band 6p25.3 — in an intron of GMDS.
What each result means
A/ANo copy of the version the research linked to Glaucoma (primary open-angle). This is the starting point the study compared everyone against.
A/GOne copy of the version the research linked to Glaucoma (primary open-angle). That is a smaller link than two copies.
G/GTwo copies of the version the research linked to Glaucoma (primary open-angle). That is the strongest link of the three results. A link in a study is not a diagnosis.
Nature communications · 2018 · PMID 29891935 · open access
Questions about rs9392348
What is rs9392348?
rs9392348 is a single position in the genome, in or near the GMDS gene. Published research associates it with glaucoma (primary open-angle). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
What conditions is rs9392348 linked to?
On MyGeneLog this position is linked to Glaucoma. The research behind each link, and its sources, are set out on that condition page.
Does having rs9392348 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 rs9392348 come from?
GWAS Catalog, Nat Commun 2018, PMID:29891935. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
0 241218237Reads by AI crawlersClaude1ChatGPT0Google · Gemini2Perplexity1Meta AI8Microsoft · Copilot0Amazon2Apple3China (ByteDance, Huawei, Baidu…)0Others7Total24Counted 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.