0 1718224Reads by AI crawlersClaude0ChatGPT0Google · Gemini1Perplexity0Meta AI8Microsoft · Copilot0Amazon2Apple2China (ByteDance, Huawei, Baidu…)0Others4Total17Counted 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.
Stands on its own.
Nothing else here links to this position yet — but the page above is the point: what the
research found, what each genotype means, and where it came from, in language you can
read. Links to conditions, drugs and the senses appear automatically if we write them.
What the study found
Who was studied 3,057 Black individuals, 10,769 European ancestry individuals.
The effect
Each copy of the A allele shifted the measure 0.07 higher (95% confidence interval 0.045-0.095); p = 8 × 10−9.
How common The A allele had a frequency of about 74% in the people studied.
Where it sits Chromosome 7, band 7p22.1 — inside ACTB.
What each result means
A/ATwo copies of the version the research linked to Global electrical heterogeneity phenotypes. That is the strongest link of the three results. A link in a study is not a diagnosis.
A/TOne copy of the version the research linked to Global electrical heterogeneity phenotypes. That is a smaller link than two copies.
T/TNo copy of the version the research linked to Global electrical heterogeneity phenotypes. This is the starting point the study compared everyone against.
Journal of the American Heart Association · 2018 · PMID 29622589 · open access
Questions about rs2098226
What is rs2098226?
rs2098226 is a single position in the genome, in or near the ACTB gene. Published research associates it with global electrical heterogeneity phenotypes. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs2098226 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 rs2098226 come from?
GWAS Catalog, J Am Heart Assoc 2018, PMID:29622589. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
0 1718224Reads by AI crawlersClaude0ChatGPT0Google · Gemini1Perplexity0Meta AI8Microsoft · Copilot0Amazon2Apple2China (ByteDance, Huawei, Baidu…)0Others4Total17Counted 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.
Global electrical heterogeneity phenotypes (rs2098226). MyGeneLog™. https://www.mygenelog.com/variants/rs2098226