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Asthma

IVL · rs115813648

Where this position leads

Condition: Asthma

rs115813648 Condition: Asthma Asthma Condition rs115813648 rs115813648 IVL

What the study found

Who was studied 46,802 European ancestry cases, 347,481 European ancestry controls; replicated in 23,948 European and unknown ancestry cases, 118,538 European and unknown ancestry controls.

The effect Each copy of the C allele carried 1.17 times the odds of Asthma (95% confidence interval 1.13-1.21); p = 2 × 10−13.

How common The C allele had a frequency of about 2% in the people studied.

Where it sits Chromosome 1, band 1q21.3 — in the 3′ untranslated region of LINC01527.

What each result means

C/C Two copies of the version the research linked to Asthma. That is the strongest link of the three results. A link in a study is not a diagnosis.
C/T One copy of the version the research linked to Asthma. That is a smaller link than two copies.
T/T No copy of the version the research linked to Asthma. This is the starting point the study compared everyone against.
Source

Questions about rs115813648

What is rs115813648?

rs115813648 is a single position in the genome, in or near the IVL gene. Published research associates it with 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 rs115813648 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 rs115813648 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 rs115813648 come from?

GWAS Catalog, The European respiratory journal 2019, PMID:31619474. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.

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.

Asthma (rs115813648). MyGeneLog™. https://www.mygenelog.com/variants/rs115813648

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