Coronary artery disease and triglyceride levels (multivariate analysis)
FBRSL1 · rs12423664
0 21161238Reads by AI crawlersClaude0ChatGPT0Google · Gemini0Perplexity1Meta AI6Microsoft · Copilot1Amazon2Apple3China (ByteDance, Huawei, Baidu…)0Others8Total21Counted 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 122,733 coronary artery disease cases, 424,528 coronary artery disease controls, 188,577 individuals.
The effect
The reported allele is A; the catalogue records no effect size
; p = 1 × 10−8.
How common The A allele had a frequency of about 13% in the people studied.
Where it sits Chromosome 12, band 12q24.33 — in an intron of FBRSL1.
What each result means
A/ATwo copies of the version the research linked to Coronary artery disease and triglyceride levels (multivariate analysis). 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 Coronary artery disease and triglyceride levels (multivariate analysis). That is a smaller link than two copies.
G/GNo copy of the version the research linked to Coronary artery disease and triglyceride levels (multivariate analysis). This is the starting point the study compared everyone against.
Circulation. Genomic and precision medicine · 2018 · PMID 30525989
Questions about rs12423664
What is rs12423664?
rs12423664 is a single position in the genome, in or near the FBRSL1 gene. Published research associates it with coronary artery disease and triglyceride levels (multivariate analysis). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
What conditions is rs12423664 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 rs12423664 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 rs12423664 come from?
GWAS Catalog, Circ Genom Precis Med 2018, PMID:30525989. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
0 21161238Reads by AI crawlersClaude0ChatGPT0Google · Gemini0Perplexity1Meta AI6Microsoft · Copilot1Amazon2Apple3China (ByteDance, Huawei, Baidu…)0Others8Total21Counted 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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