Variants linked to Coronary Artery Disease

Continuously updated · newest added Oct 22, 2026

258 positions on this site are linked to Coronary Artery Disease, out of 107,348 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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Sensitive

Coronary artery disease

NBEAL1 · rs6728861

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Sensitive

Coronary artery disease

MRAS · rs185244

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Sensitive

Coronary artery disease

PECAM1 · rs9892152

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Sensitive

Coronary artery disease

ATP1B1 · rs1892094

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Sensitive

Coronary artery disease

LOC100506393 · rs10841443

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Sensitive

Coronary artery disease

COL4A2 · rs9515203

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Sensitive

Coronary artery disease

B9D2 · rs4803455

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Sensitive

Coronary artery disease

near MC4R · rs663640

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Sensitive

Coronary artery disease

FLT1 · rs9319428

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Sensitive

Coronary artery disease

LOC553103 · rs273909

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Sensitive

Coronary artery disease

AS3MT · rs3740390

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Sensitive

Coronary artery disease

GUCY1A3 · rs7692387

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Sensitive

Coronary artery disease

CETP · rs12149545

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Sensitive

Coronary artery disease

ARHGAP26 · rs246600

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Sensitive

Coronary artery disease

PRIM2 · rs71566846

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Sensitive

Coronary artery disease

FNDC3B · rs12897

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Sensitive

Coronary artery disease

near N4BP2L2 · rs7998440

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Sensitive

Coronary artery disease

MAP3K7CL · rs2832227

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Sensitive

Coronary artery disease

MAP1S · rs7251815

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Sensitive

Coronary artery disease

DHX58 · rs2074164

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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.