Variants linked to Asthma

Continuously updated · newest added Oct 24, 2026

342 positions on this site are linked to Asthma, out of 113,447 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

Asthma

PRDM16 · rs79408112

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Standard

Asthma (childhood onset)

ITGB6 · rs4473914

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Standard

Asthma

EEFSEC · rs2811373

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Standard

Asthma

LRRC32 · rs12718488

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Standard

Asthma

RCOR1 · rs59457020

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Standard

Asthma

TCP11 · rs28522747

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Sensitive

Allergic disease (asthma, hay fever or eczema)

GATA3 · rs11255968

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Standard

Endometriosis or asthma (pleiotropy)

RUNX1 · rs8129889

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Standard

Asthma (childhood onset)

near DNAJB6P1 · rs7927044

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Standard

Asthma

LINC01807 · rs3732192

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Standard

Endometriosis or asthma (pleiotropy)

SMAD3 · rs28360855

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Standard

Endometriosis or asthma (pleiotropy)

PPP1R3B-DT · rs17658270

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Standard

Asthma

near RNA5SP214 · rs144763329

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Standard

Asthma

near LRRC3B · rs9836823

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Standard

Asthma

CRTAP · rs79337446

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Standard

Asthma

FPR3 · rs62108951

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Standard

Asthma

TMEM272 · rs1543525

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Standard

Endometriosis or asthma (pleiotropy)

RUNX1 · rs8133814

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Standard

Asthma

near MAGOH3P · rs79509103

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Standard

Asthma

near TSLP · rs62375550

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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.