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/FVC ratio

GRIP1 · rs74910874

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Standard

Post bronchodilator FEV1/FVC ratio

CELF4 · rs188403275

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Standard

Post bronchodilator FEV1

BC127192 · rs117767473

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Standard

Post bronchodilator FEV1

near FOXQ1 · rs147846168

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Standard

Post bronchodilator FEV1

near P2RY1 · rs181840477

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Standard

Post bronchodilator FEV1

near P2RY1 · rs148200394

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Standard

Post bronchodilator FEV1

COBL · rs114659987

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Standard

Post bronchodilator FEV1

near COBL · rs186739251

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Standard

Post bronchodilator FEV1/FVC ratio

near MMP3 · rs17361668

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Standard

Post bronchodilator FEV1/FVC ratio

PPP4R4 · rs112458284

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Standard

Post bronchodilator FEV1/FVC ratio

near HHIP · rs62346060

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Standard

Post bronchodilator FEV1/FVC ratio

near MMP12 · rs72981698

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Standard

Post bronchodilator FEV1/FVC ratio

near MMP3 · rs72981683

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Standard

Post bronchodilator FEV1/FVC ratio

near MMP3 · rs116187470

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Standard

Post bronchodilator FEV1/FVC ratio

near TGFB2 · rs72738847

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Standard

Post bronchodilator FEV1/FVC ratio

near MMP3 · rs72981675

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Standard

Post bronchodilator FEV1/FVC ratio

near MMP12 · rs72983508

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Standard

Post bronchodilator FEV1/FVC ratio

near MMP3 · rs114176245

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Standard

Post bronchodilator FEV1/FVC ratio

near HHIP · rs11724319

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Standard

Post bronchodilator FEV1/FVC ratio

RIN3 · rs117068593

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Showing 20 of 264 · page 6 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.