2 40321423223Reads by AI crawlersClaude3ChatGPT2Google · Gemini0Perplexity1Meta AI4Microsoft · Copilot0Amazon2Apple3China (ByteDance, Huawei, Baidu…)2ByteDance (Doubao)2Others23Total40Counted 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 4,139 European and other ancestry p.Phe508del homozygote cases, 2,226 European and other ancestry cases.
The effect
The reported allele is C; the catalogue records no effect size
; p = 5 × 10−6.
How common The C allele had a frequency of about 48% in the people studied.
Where it sits Chromosome X, band Xq23 — between genes, 42 kb from AGTR2.
What each result means
C/CTwo copies of the version the research linked to Lung disease severity in cystic fibrosis. 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 Lung disease severity in cystic fibrosis. That is a smaller link than two copies.
T/TNo copy of the version the research linked to Lung disease severity in cystic fibrosis. This is the starting point the study compared everyone against.
Nature communications · 2015 · PMID 26417704 · open access
Questions about rs7879546
What is rs7879546?
rs7879546 is a single position in the genome, in or near the AGTR2 gene. Published research associates it with lung disease severity in cystic fibrosis. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
What conditions is rs7879546 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 rs7879546 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 rs7879546 come from?
GWAS Catalog, Nat Commun 2015, PMID:26417704. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
2 40321423223Reads by AI crawlersClaude3ChatGPT2Google · Gemini0Perplexity1Meta AI4Microsoft · Copilot0Amazon2Apple3China (ByteDance, Huawei, Baidu…)2ByteDance (Doubao)2Others23Total40Counted 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.
Lung disease severity in cystic fibrosis (rs7879546). MyGeneLog™. https://www.mygenelog.com/variants/rs7879546