Variants linked to Pulmonary Function (Lung Capacity)

Continuously updated · newest added Oct 23, 2026

264 positions on this site are linked to Pulmonary Function (Lung Capacity), out of 112,191 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 Pulmonary Function (Lung Capacity)

Standard

Post bronchodilator FEV1

near COL1A2 · rs189936349

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Standard

Post bronchodilator FEV1/FVC ratio

CHRNB4 · rs1996371

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Standard

Post bronchodilator FEV1/FVC ratio

near GYPA · rs1394998

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Standard

Post bronchodilator FEV1

near IREB2 · rs951985

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Standard

Post bronchodilator FEV1

IREB2 · rs17484524

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Standard

Post bronchodilator FEV1

CHRNA3 · rs141518190

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Standard

Post bronchodilator FEV1

CHRNA5 · rs55853698

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Standard

Post bronchodilator FEV1

near HHIP · rs6833979

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Standard

Post bronchodilator FEV1

CHRNA5 · rs7180002

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Standard

Post bronchodilator FEV1

near PSMA4 · rs56117933

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Standard

Post bronchodilator FEV1

CHRNA3 · rs189218934

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Standard

Post bronchodilator FEV1

near HHIP · rs1489760

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Standard

Post bronchodilator FEV1

near HHIP · rs1980057

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Standard

Post bronchodilator FEV1

near HHIP · rs1489763

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Standard

Post bronchodilator FEV1

CHRNA3 · rs28669908

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Standard

Post bronchodilator FEV1

near HHIP · rs6537292

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Standard

Post bronchodilator FEV1

CHRNA5 · rs503464

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Standard

Post bronchodilator FEV1

near HHIP · rs1565330

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Standard

Post bronchodilator FEV1

near HHIP · rs13113591

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Standard

Post bronchodilator FEV1

PSMA4 · rs58365910

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Showing 20 of 264 · page 7 of 14

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.