AR-C124910XX levels in individuals with acute coronary syndromes treated with ticagrelor
SLCO1A2 · rs113681054
2 443225122225Reads by AI crawlersClaude3ChatGPT2Google · Gemini0Perplexity2Meta AI5Microsoft · Copilot1Amazon2Apple2China (ByteDance, Huawei, Baidu…)2ByteDance (Doubao)2Others25Total44Counted 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 1,794 European ancestry cases, 18 African and Asian ancestry cases; replicated in 1,922 European ancestry cases, 19 African and Asian ancestry cases.
The effect
Each copy of the T allele shifted the measure 0.062 higher (95% confidence interval 0.044-0.08); p = 4 × 10−13.
How common The T allele had a frequency of about 18% in the people studied.
Where it sits Chromosome 12, band 12p12.1 — inside LOC124902895.
What each result means
C/CNo copy of the version the research linked to AR-C124910XX levels in individuals with acute coronary syndromes treated with ticagrelor. This is the starting point the study compared everyone against.
C/TOne copy of the version the research linked to AR-C124910XX levels in individuals with acute coronary syndromes treated with ticagrelor. That is a smaller link than two copies.
T/TTwo copies of the version the research linked to AR-C124910XX levels in individuals with acute coronary syndromes treated with ticagrelor. That is the strongest link of the three results. A link in a study is not a diagnosis.
Papers in Europe PMC whose title or abstract names both this rsID and that subject. A shared paper means somebody wrote about the two together — it is not a claim that this position explains the subject.
Questions about rs113681054
What is rs113681054?
rs113681054 is a single position in the genome, in or near the SLCO1A2 gene. Published research associates it with ar-c124910xx levels in individuals with acute coronary syndromes treated with ticagrelor. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
What conditions is rs113681054 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.
What do people read about alongside rs113681054?
Subjects that appear in the title or abstract of the same papers as this rsID include heart and circulation (1 papers). A shared paper means somebody wrote about the two together; it is not a claim that this position explains the topic.
Does having rs113681054 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 rs113681054 come from?
GWAS Catalog, Eur Heart J 2015, PMID:25935875. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
2 443225122225Reads by AI crawlersClaude3ChatGPT2Google · Gemini0Perplexity2Meta AI5Microsoft · Copilot1Amazon2Apple2China (ByteDance, Huawei, Baidu…)2ByteDance (Doubao)2Others25Total44Counted 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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AR-C124910XX levels in individuals with acute coronary syndromes treated with ticagrelor (rs113681054). MyGeneLog™. https://www.mygenelog.com/variants/rs113681054