Eudesmic acid (3,4,5-trimethoxybenzoic acid) levels in coronary artery disease
EDNRB-AS1 · rs9530695
0 422Reads by AI crawlersClaude0ChatGPT0Google · Gemini0Perplexity0Meta AI0Microsoft · Copilot0Amazon2Apple0China (ByteDance, Huawei, Baidu…)0Others2Total4Counted 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 1,551 Han Chinese ancestry individuals.
The effect
Each copy of the C allele shifted the measure 2.5 higher (95% confidence interval 1.87-3.13); p = 6 × 10−15.
How common The C allele had a frequency of about 94% in the people studied.
Where it sits Chromosome 13, band 13q22.3 — in an intron of EDNRB-AS1.
What each result means
C/CTwo copies of the version the research linked to Eudesmic acid (3,4,5-trimethoxybenzoic acid) levels in coronary artery disease. That is the strongest link of the three results. A link in a study is not a diagnosis.
C/GOne copy of the version the research linked to Eudesmic acid (3,4,5-trimethoxybenzoic acid) levels in coronary artery disease. That is a smaller link than two copies.
G/GNo copy of the version the research linked to Eudesmic acid (3,4,5-trimethoxybenzoic acid) levels in coronary artery disease. This is the starting point the study compared everyone against.
Clinical and translational medicine · 2021 · PMID 33634981 · open access
Questions about rs9530695
What is rs9530695?
rs9530695 is a single position in the genome, in or near the EDNRB-AS1 gene. Published research associates it with eudesmic acid (3,4,5-trimethoxybenzoic acid) levels in coronary artery disease. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
What conditions is rs9530695 linked to?
On MyGeneLog this position is linked to Coronary Artery Disease. The research behind each link, and its sources, are set out on that condition page.
Does having rs9530695 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 rs9530695 come from?
GWAS Catalog, Clinical and translational medicine 2021, PMID:33634981. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
0 422Reads by AI crawlersClaude0ChatGPT0Google · Gemini0Perplexity0Meta AI0Microsoft · Copilot0Amazon2Apple0China (ByteDance, Huawei, Baidu…)0Others2Total4Counted 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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