Variants linked to Asthma

Continuously updated · newest added Oct 24, 2026

342 positions on this site are linked to Asthma, out of 113,615 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

Standard

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

RBBP8 · rs112104755

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Standard

Asthma

GLIS3 · rs7041606

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Standard

Asthma (childhood onset)

IL6 · rs34880821

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Sensitive

Asthma in any disease

IP6K3 · rs28607030

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Standard

Asthma

PTPRC · rs17668708

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Standard

Asthma

CDK12 · rs801429

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Standard

Asthma

near GADD45G · rs7030895

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Sensitive

Allergic disease (asthma, hay fever or eczema)

JAK2 · rs16922576

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Standard

Asthma

POLR1HASP · rs886997

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Standard

Asthma

LINC02676 · rs827637

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Sensitive

Allergic disease (asthma, hay fever or eczema)

PTPRK · rs35469349

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Sensitive

Asthma in any disease

LRP1 · rs17547610

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Standard

Asthma

AP1S3 · rs13383994

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Standard

Asthma (adult onset)

TEX41 · rs12617922

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Standard

Asthma

C6orf100 · rs114357009

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Standard

Asthma

NSD1 · rs12187932

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Standard

Asthma

ORMDL3 · rs7216389

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Standard

Asthma

HLA-DPA1 · rs35449774

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Standard

Pediatric asthma

LINC00299 · rs2561999

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Standard

Asthma

NFKBIA · rs2007960

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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.