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 112,023 published in total. Each was published only after passing the same quality gate; being on this list is an association, not a diagnosis.

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Standard

Post bronchodilator FEV1

AGPHD1 · rs12439240

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Standard

Post bronchodilator FEV1

CHRNB4 · rs12441088

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Standard

Post bronchodilator FEV1

near HHIP · rs35937742

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Standard

Post bronchodilator FEV1

PSMA4 · rs3813570

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Standard

Post bronchodilator FEV1

near GYPA · rs4835177

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Standard

Post bronchodilator FEV1

FAM13A · rs7682317

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Standard

Post bronchodilator FEV1

near HHIP · rs1490151

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Standard

Post bronchodilator FEV1

CHRNA3 · rs147144681

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Standard

Post bronchodilator FEV1/FVC ratio

near HHIP · rs1813903

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Standard

Post bronchodilator FEV1/FVC ratio

CHRNA5 · rs72740964

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Standard

Post bronchodilator FEV1/FVC ratio

AGPHD1 · rs34684276

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Standard

Pulmonary function (smoking interaction)

SOX9 · rs11654749

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Standard

Pulmonary function (smoking interaction)

HLA-DQA2 · rs7764819

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Standard

Pulmonary function

ADAM19 · rs2277027

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Standard

Pulmonary function

HTR4 · rs11168048

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Standard

Pulmonary function

ZKSCAN3 · rs6903823

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Standard

Pulmonary function

MMP15 · rs12447804

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Standard

Pulmonary function

ARMC2 · rs2798641

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Standard

Pulmonary function

HHIP · rs13147758

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Standard

Pulmonary function

HHIP · rs12504628

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Showing 20 of 264 · page 13 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.