0 1122223Reads by AI crawlersClaude0ChatGPT0Google · Gemini2Perplexity0Meta AI0Microsoft · Copilot0Amazon2Apple2China (ByteDance, Huawei, Baidu…)2ByteDance (Doubao)2Others3Total11Counted 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 3,382,012 European ancestry, East Asian ancestry, Hispanic or Latin American, African ancestry individuals.
The effect
Each copy of the A allele shifted the measure 0.0102 lower (95% confidence interval 0.0085-0.0119); p = 8 × 10−32.
How common The A allele had a frequency of about 28% in the people studied.
Where it sits Chromosome 18, band 18q12.1 — between genes, 174.5 kb from PA2G4P3.
What each result means
A/ATwo copies of the version the research linked to Smoking initiation. 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 Smoking initiation. That is a smaller link than two copies.
G/GNo copy of the version the research linked to Smoking initiation. This is the starting point the study compared everyone against.
rs10853676 is a single position in the genome, in or near the near PA2G4P3 gene. Published research associates it with smoking initiation. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs10853676 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 rs10853676 come from?
GWAS Catalog, Nature 2022, PMID:36477530. 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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