Variants linked to Chronic Obstructive Pulmonary Disease (COPD)

Continuously updated · newest added Oct 25, 2026

57 positions on this site are linked to Chronic Obstructive Pulmonary Disease (COPD), out of 117,018 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 Chronic Obstructive Pulmonary Disease (COPD)

Sensitive

Chronic obstructive pulmonary disease

ADGRG6 · rs11155242

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Sensitive

Chronic obstructive pulmonary disease

C1orf87 · rs72673419

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Sensitive

Chronic obstructive pulmonary disease

CDC123 · rs2001546

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Sensitive

Chronic obstructive pulmonary disease

CACNA2D3 · rs17759204

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Sensitive

Chronic obstructive pulmonary disease

THSD4 · rs2119568

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Sensitive

Chronic lung diseases including COPD, Emphysema and Bronchitis

near KRT18P51 · rs13148031

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Sensitive

Chronic lung diseases including COPD, Emphysema and Bronchitis

CHRNA4 · rs151176846

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Sensitive

Chronic obstructive pulmonary disease

NPNT · rs11727735

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Sensitive

Response to bronchodilator in chronic obstructive pulmonary disease (change in FEV1)

SGCD · rs10056066

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Sensitive

Response to bronchodilator in chronic obstructive pulmonary disease (change in FEV1)

CDH13 · rs114132812

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Sensitive

Response to bronchodilator in chronic obstructive pulmonary disease (change in FEV1)

PITPNA · rs140948272

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Standard

Post bronchodilator FEV1

CHRNA3 · rs147144681

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Standard

Post bronchodilator FEV1/FVC ratio

CHRNA5 · rs72740964

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Standard

Post bronchodilator FEV1/FVC ratio

near HHIP · rs1813903

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Standard

Post bronchodilator FEV1/FVC ratio

AGPHD1 · rs34684276

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Sensitive

Chronic obstructive pulmonary disease (severe)

FAM13A · rs4416442

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Sensitive

Chronic obstructive pulmonary disease (severe)

TGFB2 · rs4846480

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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.