0 6123Reads by AI crawlersClaude0ChatGPT0Google · Gemini0Perplexity1Meta AI0Microsoft · Copilot0Amazon2Apple0China (ByteDance, Huawei, Baidu…)0Others3Total6Counted 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 394,642 European ancestry individuals.
The effect
Each copy of the A allele shifted the measure 0.0171 higher (95% confidence interval 0.012-0.022); p = 5 × 10−13.
How common The A allele had a frequency of about 20% in the people studied.
Where it sits Chromosome 11, band 11q23.3 — between genes, 3.5 kb from SETP16.
What each result means
A/ATwo copies of the version the research linked to Eosinophill percentage (UKB data field 30210). That is the strongest link of the three results. A link in a study is not a diagnosis.
A/GOne copy of the version the research linked to Eosinophill percentage (UKB data field 30210). That is a smaller link than two copies.
G/GNo copy of the version the research linked to Eosinophill percentage (UKB data field 30210). This is the starting point the study compared everyone against.
Nature genetics · 2025 · PMID 39789286 · open access
Questions about rs79504890
What is rs79504890?
rs79504890 is a single position in the genome, in or near the near SETP16 gene. Published research associates it with eosinophill percentage (ukb data field 30210). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
What conditions is rs79504890 linked to?
On MyGeneLog this position is linked to Celiac Disease. The research behind each link, and its sources, are set out on that condition page.
Does having rs79504890 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 rs79504890 come from?
GWAS Catalog, Nature genetics 2025, PMID:39789286. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
0 6123Reads by AI crawlersClaude0ChatGPT0Google · Gemini0Perplexity1Meta AI0Microsoft · Copilot0Amazon2Apple0China (ByteDance, Huawei, Baidu…)0Others3Total6Counted 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.
Eosinophill percentage (UKB data field 30210) (rs79504890). MyGeneLog™. https://www.mygenelog.com/variants/rs79504890