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Asthma

LRRC32 · rs7130588

Where this position leads

Condition: Asthma

rs7130588 Condition: Asthma Asthma Condition rs7130588 rs7130588 LRRC32

What each result means

A/A Published research associates this genotype with typical/baseline likelihood of Asthma — no copies of the reported risk allele. (GWAS Catalog, Lancet 2011, PMID:21907864)
A/G Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Asthma. (GWAS Catalog, Lancet 2011, PMID:21907864)
G/G Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Asthma compared to the general population. (GWAS Catalog, Lancet 2011, PMID:21907864)

Source: GWAS Catalog, Lancet 2011, PMID:21907864

What people read about alongside this

Papers in Europe PMC whose title or abstract names both this rsID and that subject. A shared paper means somebody wrote about the two together — it is not a claim that this position explains the subject.

Questions about rs7130588

What is rs7130588?

rs7130588 is a single position in the genome, in or near the LRRC32 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 rs7130588 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.

What do people read about alongside rs7130588?

Subjects that appear in the title or abstract of the same papers as this rsID include allergies (1 papers). A shared paper means somebody wrote about the two together; it is not a claim that this position explains the topic.

Does having rs7130588 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 rs7130588 come from?

GWAS Catalog, Lancet 2011, PMID:21907864. 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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