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Who was studied 4,235 African American Afro-Caribbean cases, 5,283 African American Afro-Caribbean controls, 2774 Hispanic cases, 2,362 Hispanic controls.
The effect
Each copy of the T allele carried 1.26 times the odds of Adult asthma (95% confidence interval 1.17-1.37); p = 3 × 10−8.
How common The T allele had a frequency of about 12% in the people studied.
Where it sits Chromosome 8, band 8p23.2 — in an intron of LINC03021.
What each result means
C/CNo copy of the version the research linked to Adult asthma. This is the starting point the study compared everyone against.
C/TOne copy of the version the research linked to Adult asthma. That is a smaller link than two copies.
T/TTwo copies of the version the research linked to Adult asthma. That is the strongest link of the three results. A link in a study is not a diagnosis.
Nature communications · 2019 · PMID 30787307 · open access
Questions about rs13277810
What is rs13277810?
rs13277810 is a single position in the genome, in or near the LOC101927815 gene. Published research associates it with adult asthma. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
What conditions is rs13277810 linked to?
On MyGeneLog this position is linked to Asthma. The research behind each link, and its sources, are set out on that condition page.
Does having rs13277810 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 rs13277810 come from?
GWAS Catalog, Nature communications 2019, PMID:30787307. 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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