Plasma proprotein convertase subtilisin/kexin type 9 levels in stable coronary artery disease
FBXL18 · rs6957201
0 110Reads by AI crawlersClaude1ChatGPT0Google · Gemini0Perplexity0Meta AI0Microsoft · Copilot0Amazon0Apple0China (ByteDance, Huawei, Baidu…)0Others0Total1Counted 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 2,022 European ancestry individuals without statin treatment, 1,268 European ancestry individuals with statin treatment.
The effect
Each copy of the C allele shifted the measure 0.163 lower (95% confidence interval 0.11-0.22); p = 7 × 10−9.
How common The C allele had a frequency of about 97% in the people studied.
Where it sits Chromosome 7, band 7p22.1 — in an intron of LINC03073.
What each result means
C/CTwo copies of the version the research linked to Plasma proprotein convertase subtilisin/kexin type 9 levels in stable coronary artery disease. That is the strongest link of the three results. A link in a study is not a diagnosis.
C/TOne copy of the version the research linked to Plasma proprotein convertase subtilisin/kexin type 9 levels in stable coronary artery disease. That is a smaller link than two copies.
T/TNo copy of the version the research linked to Plasma proprotein convertase subtilisin/kexin type 9 levels in stable coronary artery disease. This is the starting point the study compared everyone against.
Circulation. Genomic and precision medicine · 2018 · PMID 29748315
Questions about rs6957201
What is rs6957201?
rs6957201 is a single position in the genome, in or near the FBXL18 gene. Published research associates it with plasma proprotein convertase subtilisin/kexin type 9 levels in stable 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 rs6957201 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 rs6957201 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 rs6957201 come from?
GWAS Catalog, Circulation. Genomic and precision medicine 2018, PMID:29748315. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
0 110Reads by AI crawlersClaude1ChatGPT0Google · Gemini0Perplexity0Meta AI0Microsoft · Copilot0Amazon0Apple0China (ByteDance, Huawei, Baidu…)0Others0Total1Counted 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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Plasma proprotein convertase subtilisin/kexin type 9 levels in stable coronary artery disease (rs6957201). MyGeneLog™. https://www.mygenelog.com/variants/rs6957201