Variants linked to Asthma

Continuously updated · newest added Oct 24, 2026

344 positions on this site are linked to Asthma, out of 113,825 published in total. Each was published only after passing the same quality gate; being on this list is an association, not a diagnosis.

← Back to Asthma

Sensitive

Allergic disease (asthma, hay fever or eczema)

near LAYN · rs11213941

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Standard

Asthma

RUNX1 · rs2242900

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Standard

Asthma

RAD50 · rs6596086

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Standard

Asthma

CD28 · rs4673259

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Standard

Nonatopic asthma and/or BMI

near MTCO3P1 · rs9275570

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Standard

Asthma

CD247 · rs1617333

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Standard

Asthma

near LINC02676 · rs7898135

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Standard

Asthma

HCG24 · rs6901830

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Standard

Asthma

CAMK4 · rs6594500

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Standard

Asthma

ABCB5 · rs7802450

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Sensitive

Allergic disease (asthma, hay fever or eczema)

RAD50 · rs3091307

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Standard

Asthma

RORA · rs7183955

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Standard

Asthma (childhood onset)

KIF3A · rs2051809

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Sensitive

Allergic disease (asthma, hay fever or eczema)

SLC25A46 · rs1814576

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Standard

Asthma

HLA-DRA · rs146618240

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Standard

Asthma

HLA-DRB6 · rs115468973

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Standard

Asthma

near LINC02676 · rs72784452

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Standard

Asthma

RAD50 · rs60156285

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Standard

Asthma

MIR5708 · rs2221641

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Standard

Asthma

BACH2 · rs62408233

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Showing 20 of 344 · page 9 of 18

Questions about variants on this site

What is a "variant" page on this site?

One specific position in the genome (an rsID), explained in plain language with what published research has found it linked to, and how strong that link actually is.

Where does new variant data come from?

The public GWAS Catalog, checked every twenty minutes, plus variants added manually after research review. Every one passes the same quality gate before publishing.

Does being listed here mean a variant causes a condition?

No. Listing reflects an association from published research, not a diagnosis or a cause. Most common variants shift probability modestly rather than determining an outcome.

Can I search this list by gene or rsID?

Yes — the search box above matches gene symbols and rsIDs as well as trait names.