1 16115225Reads by AI crawlersClaude1ChatGPT0Google · Gemini1Perplexity0Meta AI5Microsoft · Copilot0Amazon2Apple2Others5Total16Counted 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 170,672 European ancestry individuals.
The effect
Each copy of the T allele shifted the measure 0.0272 lower (95% confidence interval 0.018-0.036); p = 1 × 10−9.
How common The T allele had a frequency of about 21% in the people studied.
Where it sits Chromosome 12, band 12p13.33 — in an intron of RAD52.
What each result means
C/CPublished research associates this genotype with typical/baseline likelihood of Neutrophil percentage of granulocytes — no copies of the reported risk allele.
C/TPublished research associates this genotype (one copy of the reported risk allele) with an intermediate association with Neutrophil percentage of granulocytes.
T/TPublished research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Neutrophil percentage of granulocytes compared to the general population.
rs11571404 is a single position in the genome, in or near the RAD52 gene. Published research associates it with neutrophil percentage of granulocytes. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
What conditions is rs11571404 linked to?
On MyGeneLog this position is linked to Blood Cell Counts. The research behind each link, and its sources, are set out on that condition page.
Does having rs11571404 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 rs11571404 come from?
GWAS Catalog, Cell 2016, PMID:27863252. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
1 16115225Reads by AI crawlersClaude1ChatGPT0Google · Gemini1Perplexity0Meta AI5Microsoft · Copilot0Amazon2Apple2Others5Total16Counted 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.
Neutrophil percentage of granulocytes (rs11571404). MyGeneLog™. https://www.mygenelog.com/variants/rs11571404