4 4762125223123Reads by AI crawlersClaude6ChatGPT2Google · Gemini1Perplexity2Meta AI5Microsoft · Copilot2Amazon2Apple3China (ByteDance, Huawei, Baidu…)1ByteDance (Doubao)1Others23Total47Counted 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 4,627 European ancestry individuals; replicated in 9,316 European ancestry individuals.
The effect
Each copy of the G allele shifted the measure 4.65 10^9/l higher (95% confidence interval 3.32-5.98); p = 8 × 10−12.
Where it sits Chromosome 12, band 12q24.13 — in an intron of PTPN11.
What each result means
A/ANo copy of the version the research linked to Hematological parameters. This is the starting point the study compared everyone against.
A/GOne copy of the version the research linked to Hematological parameters. That is a smaller link than two copies.
G/GTwo copies of the version the research linked to Hematological parameters. That is the strongest link of the three results. A link in a study is not a diagnosis.
Papers in Europe PMC whose title or abstract names both this rsID and that subject. A shared paper means somebody wrote about the two together — it is not a claim that this position explains the subject.
Questions about rs11066301
What is rs11066301?
rs11066301 is a single position in the genome, in or near the PTPN11 gene. Published research associates it with hematological parameters. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
What conditions is rs11066301 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.
What do people read about alongside rs11066301?
Subjects that appear in the title or abstract of the same papers as this rsID include heart and circulation (1 papers). A shared paper means somebody wrote about the two together; it is not a claim that this position explains the topic.
Does having rs11066301 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 rs11066301 come from?
GWAS Catalog, Nat Genet 2009, PMID:19820697. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
4 4762125223123Reads by AI crawlersClaude6ChatGPT2Google · Gemini1Perplexity2Meta AI5Microsoft · Copilot2Amazon2Apple3China (ByteDance, Huawei, Baidu…)1ByteDance (Doubao)1Others23Total47Counted 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.
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