Lung disease severity in cystic fibrosis with pancreatic insufficiency
near AGTR2 · rs12009976
0 312Reads by AI crawlersClaude0ChatGPT0Google · Gemini0Perplexity0Meta AI0Microsoft · Copilot0Amazon1Apple0China (ByteDance, Huawei, Baidu…)0Others2Total3Counted 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 7,437 European ancestry individuals, 403 individuals.
The effect
Each copy of the A allele shifted the measure 0.08 higher; p = 6 × 10−12.
How common The A allele had a frequency of about 49% in the people studied.
Where it sits Chromosome X, band Xq23 — between genes, 55.3 kb from AGTR2.
What each result means
A/ATwo copies of the version the research linked to Lung disease severity in cystic fibrosis with pancreatic insufficiency. 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 Lung disease severity in cystic fibrosis with pancreatic insufficiency. That is a smaller link than two copies.
G/GNo copy of the version the research linked to Lung disease severity in cystic fibrosis with pancreatic insufficiency. This is the starting point the study compared everyone against.
American journal of respiratory and critical care medicine · 2023 · PMID 36921087
Questions about rs12009976
What is rs12009976?
rs12009976 is a single position in the genome, in or near the near AGTR2 gene. Published research associates it with lung disease severity in cystic fibrosis with pancreatic insufficiency. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
What conditions is rs12009976 linked to?
On MyGeneLog this position is linked to Cystic Fibrosis. The research behind each link, and its sources, are set out on that condition page.
Does having rs12009976 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 rs12009976 come from?
GWAS Catalog, American journal of respiratory and critical care medicine 2023, PMID:36921087. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
0 312Reads by AI crawlersClaude0ChatGPT0Google · Gemini0Perplexity0Meta AI0Microsoft · Copilot0Amazon1Apple0China (ByteDance, Huawei, Baidu…)0Others2Total3Counted 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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Lung disease severity in cystic fibrosis with pancreatic insufficiency (rs12009976). MyGeneLog™. https://www.mygenelog.com/variants/rs12009976