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

ZHX3 · rs6129767

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Sensitive

Coronary artery disease

BCAS3 · rs8080784

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Sensitive

Coronary artery disease

CFDP1 · rs4888378

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Sensitive

Coronary artery disease

near DYM · rs833509

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Sensitive

Coronary artery disease

MORF4L1 · rs6495335

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Sensitive

Coronary artery disease

B9D2 · rs2288874

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Sensitive

Coronary artery disease

SMAD3 · rs56062135

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Sensitive

Coronary artery disease

near MC4R · rs34633411

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Sensitive

Coronary artery disease

NCOA6 · rs6088590

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Sensitive

Coronary artery disease

CCDC97 · rs12980942

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Sensitive

Coronary artery disease

DHX58 · rs2074158

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Sensitive

Coronary artery disease

ING1 · rs9583531

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Sensitive

Coronary artery disease

COL4A1 · rs9521678

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Sensitive

Coronary artery disease

TSPAN14 · rs12264252

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Sensitive

Coronary artery disease

near CTR9 · rs11042937

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Sensitive

Coronary artery disease

PLEKHG1 · rs12663498

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Sensitive

Coronary artery disease

SVEP1 · rs111245230

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Sensitive

Coronary artery disease

near SLC18A1 · rs11204085

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Sensitive

Coronary artery disease

ASZ1 · rs10249651

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Sensitive

Coronary artery disease

IGF2R · rs688359

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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.