Standard

Asthma (childhood onset)

GSDMB · rs2305480

Where this position leads

Condition: Asthma

rs2305480 Condition: Asthma Asthma Condition rs2305480 rs2305480 GSDMB

What each result means

A/A Published research associates this genotype with typical/baseline likelihood of Asthma (childhood onset) — no copies of the reported risk allele. (GWAS Catalog, Nat Genet 2013, PMID:24241537)
A/G Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Asthma (childhood onset). (GWAS Catalog, Nat Genet 2013, PMID:24241537)
G/G Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Asthma (childhood onset) compared to the general population. (GWAS Catalog, Nat Genet 2013, PMID:24241537)

Source: GWAS Catalog, Nat Genet 2013, PMID:24241537

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 rs2305480

What is rs2305480?

rs2305480 is a single position in the genome, in or near the GSDMB gene. Published research associates it with asthma (childhood onset). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs2305480 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 rs2305480?

Subjects that appear in the title or abstract of the same papers as this rsID include allergies (2 papers). A shared paper means somebody wrote about the two together; it is not a claim that this position explains the topic.

Does having rs2305480 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 rs2305480 come from?

GWAS Catalog, Nat Genet 2013, PMID:24241537. 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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