0 1725226Reads by AI crawlersClaude2ChatGPT0Google · Gemini0Perplexity0Meta AI0Microsoft · Copilot5Amazon2Apple2China (ByteDance, Huawei, Baidu…)0Others6Total17Counted 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 2,893 European ancestry individuals.
The effect
Each copy of the A allele shifted the measure 0.957 lower (95% confidence interval 0.88-1.03); p = 1 × 10−132.
How common The A allele had a frequency of about 89% in the people studied.
Where it sits Chromosome 17, band 17q25.1 — between genes, 15.2 kb from CD300LB.
What each result means
A/ATwo copies of the version the research linked to CMRF35-like molecule 6 levels. 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 CMRF35-like molecule 6 levels. That is a smaller link than two copies.
G/GNo copy of the version the research linked to CMRF35-like molecule 6 levels. This is the starting point the study compared everyone against.
Nature communications · 2021 · PMID 34857772 · open access
Questions about rs2089139
What is rs2089139?
rs2089139 is a single position in the genome, in or near the near CD300LB gene. Published research associates it with cmrf35-like molecule 6 levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs2089139 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 rs2089139 come from?
GWAS Catalog, Nature communications 2021, PMID:34857772. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
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