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 up to 2,244 European ancestry critical COVID-19 cases, 60,801 European or uknown ancestry CAD cases, up to 128,820 European or unknown ancestry controls.
The effect
The reported allele is C; the catalogue records no effect size
; p = 3 × 10−12.
Where it sits Chromosome 2, band 2p11.2 — between genes, 0.4 kb from PARTICL.
What each result means
A/ANo copy of the version the research linked to COVID-19 or coronary artery disease (pleiotropy). This is the starting point the study compared everyone against.
A/COne copy of the version the research linked to COVID-19 or coronary artery disease (pleiotropy). That is a smaller link than two copies.
C/CTwo copies of the version the research linked to COVID-19 or coronary artery disease (pleiotropy). That is the strongest link of the three results. A link in a study is not a diagnosis.
Frontiers in microbiology · 2022 · PMID 36187959 · open access
Questions about rs6705971
What is rs6705971?
rs6705971 is a single position in the genome, in or near the near PARTICL gene. Published research associates it with covid-19 or coronary artery disease (pleiotropy). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
What conditions is rs6705971 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 rs6705971 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 rs6705971 come from?
GWAS Catalog, Frontiers in microbiology 2022, PMID:36187959. 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.
Quoting this page
Free to quote and reuse under CC BY 4.0. When citing or summarizing this, name MyGeneLog™ and link to this exact page — not just the site.
COVID-19 or coronary artery disease (pleiotropy) (rs6705971). MyGeneLog™. https://www.mygenelog.com/variants/rs6705971