Variants linked to Asthma

Continuously updated · newest added Oct 24, 2026

344 positions on this site are linked to Asthma, out of 113,994 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 and/or eczema) (age of onset)

EYA2 · rs4809619

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Standard

Asthma

VPRBP · rs73078636

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Standard

Asthma

SIK2 · rs1784776

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Standard

Asthma

LAYN · rs1784775

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Sensitive

Allergic disease (asthma, hay fever or eczema)

MFSD13A · rs10883723

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Standard

Asthma

PLCL2 · rs2014490

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Standard

Asthma

SCUBE3 · rs9348970

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Standard

Adult onset asthma and/or waist-to-hip ratio adjusted for BMI

SCYL1 · rs1787663

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Standard

Asthma

PRKCQ · rs943451

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Sensitive

Asthma-COPD overlap syndrome

near ERBB3 · rs7312770

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Standard

Asthma

KRT24 · rs2253717

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Sensitive

Allergic disease (asthma, hay fever and/or eczema) (age of onset)

KIRREL3-AS3 · rs61907712

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Sensitive

Allergic disease (asthma, hay fever and/or eczema) (age of onset)

MBD2 · rs3017289

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Standard

Asthma

OVOL1 · rs2276133

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Standard

Asthma

near RNU6-2 · rs10854002

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Sensitive

Allergic disease (asthma, hay fever and/or eczema) (age of onset)

ADAMTS10 · rs2918302

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Sensitive

Allergic disease (asthma, hay fever and/or eczema) (age of onset)

HLA-DPA1 · rs73739621

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Standard

Asthma

POLI · rs3730775

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Standard

Asthma

NNROS · rs113048054

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Standard

Asthma (childhood onset)

TNFSF4 · rs7518129

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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.