0 2511812318Reads by AI crawlersClaude1ChatGPT0Google · Gemini0Perplexity1Meta AI8Microsoft · Copilot1Amazon2Apple3China (ByteDance, Huawei, Baidu…)1ByteDance (Doubao)1Others8Total25Counted 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 C allele shifted the measure 0.0236 higher (95% confidence interval 0.016-0.031); p = 5 × 10−10.
How common The C allele had a frequency of about 34% in the people studied.
Where it sits Chromosome 3, band 3q12.3 — between genes, 13.3 kb from TRMT10C.
What each result means
C/CTwo copies of the version the research linked to Neutrophil percentage of granulocytes. 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 Neutrophil percentage of granulocytes. That is a smaller link than two copies.
T/TNo copy of the version the research linked to Neutrophil percentage of granulocytes. This is the starting point the study compared everyone against.
rs13062095 is a single position in the genome, in or near the near TRMT10C 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 rs13062095 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 rs13062095 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 rs13062095 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.
0 2511812318Reads by AI crawlersClaude1ChatGPT0Google · Gemini0Perplexity1Meta AI8Microsoft · Copilot1Amazon2Apple3China (ByteDance, Huawei, Baidu…)1ByteDance (Doubao)1Others8Total25Counted 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 (rs13062095). MyGeneLog™. https://www.mygenelog.com/variants/rs13062095