Takes medication for coronary artery/ coronary heart disease?
MRPS6 · rs9980618
1 211122114Reads by AI crawlersClaude0ChatGPT0Google · Gemini0Perplexity1Meta AI0Microsoft · Copilot1Amazon2Apple2China (ByteDance, Huawei, Baidu…)1ByteDance (Doubao)1Others14Total21Counted 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 44,681 European ancestry cases, 270,987 European ancestry controls.
The effect
Each copy of the C allele shifted the measure 0.106 lower (95% confidence interval 0.085-0.127); p = 2 × 10−25.
How common The C allele had a frequency of about 87% in the people studied.
Where it sits Chromosome 21, band 21q22.11 — in an intron of MRPS6.
What each result means
C/CTwo copies of the version the research linked to Takes medication for coronary artery/ coronary heart 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 Takes medication for coronary artery/ coronary heart disease?. That is a smaller link than two copies.
T/TNo copy of the version the research linked to Takes medication for coronary artery/ coronary heart disease?. This is the starting point the study compared everyone against.
Science (New York, N.Y.) · 2024 · PMID 39024449 · open access
Questions about rs9980618
What is rs9980618?
rs9980618 is a single position in the genome, in or near the MRPS6 gene. Published research associates it with takes medication for coronary artery/ coronary heart 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 rs9980618 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 rs9980618 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 rs9980618 come from?
GWAS Catalog, Science (New York, N.Y.) 2024, PMID:39024449. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
1 211122114Reads by AI crawlersClaude0ChatGPT0Google · Gemini0Perplexity1Meta AI0Microsoft · Copilot1Amazon2Apple2China (ByteDance, Huawei, Baidu…)1ByteDance (Doubao)1Others14Total21Counted 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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