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The effect
Each copy of the T allele carried 1.06 times the odds of Chronic obstructive pulmonary disease (95% confidence interval 1.04-1.08); p = 4 × 10−9.
How common The T allele had a frequency of about 54% in the people studied.
Where it sits Chromosome 11, band 11p15.3 — between genes, 127 kb from BMAL1.
What each result means
C/CNo copy of the version the research linked to Chronic obstructive pulmonary disease. This is the starting point the study compared everyone against.
C/TOne copy of the version the research linked to Chronic obstructive pulmonary disease. That is a smaller link than two copies.
T/TTwo copies of the version the research linked to Chronic obstructive pulmonary disease. That is the strongest link of the three results. A link in a study is not a diagnosis.
Nature genetics · 2019 · PMID 30804561 · open access
Questions about rs4757118
What is rs4757118?
rs4757118 is a single position in the genome, in or near the ARNTL gene. Published research associates it with chronic obstructive pulmonary disease. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
What conditions is rs4757118 linked to?
On MyGeneLog this position is linked to Chronic Obstructive Pulmonary Disease (COPD). The research behind each link, and its sources, are set out on that condition page.
Does having rs4757118 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 rs4757118 come from?
GWAS Catalog, Nature genetics 2019, PMID:30804561. 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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