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 116,808 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

TESK2 · rs4660861

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Sensitive

Chronic obstructive pulmonary disease

ASTN2 · rs803923

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Sensitive

Chronic obstructive pulmonary disease

ASB1 · rs72983853

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Sensitive

Chronic obstructive pulmonary disease

THSD4 · rs12908092

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Sensitive

Chronic obstructive pulmonary disease

CCDC91 · rs11049386

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Sensitive

Chronic obstructive pulmonary disease

FGD6 · rs60129850

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Sensitive

Chronic obstructive pulmonary disease

STN1 · rs1570221

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Sensitive

Chronic obstructive pulmonary disease

RBMS3 · rs13073544

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Sensitive

Chronic obstructive pulmonary disease

EFCAB5 · rs8080772

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Sensitive

Chronic obstructive pulmonary disease

TEPP · rs8044657

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Sensitive

Chronic obstructive pulmonary disease

LINC01807 · rs62201158

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Sensitive

Chronic obstructive pulmonary disease

RPL23 · rs34727469

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Sensitive

Chronic obstructive pulmonary disease

GALK2 · rs12232354

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Sensitive

Chronic obstructive pulmonary disease

DPYD · rs114904431

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Sensitive

Chronic obstructive pulmonary disease

CHRM3 · rs11579382

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Sensitive

Chronic obstructive pulmonary disease

ARNTL · rs4757118

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Sensitive

Chronic obstructive pulmonary disease

ADAM19 · rs2287749

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Sensitive

Chronic obstructive pulmonary disease

BTC · rs4585380

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Sensitive

Chronic obstructive pulmonary disease

SOX9 · rs11655567

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Sensitive

Chronic obstructive pulmonary disease

HLA-DQA1 · rs1129740

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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.