Variants linked to Coronary Artery Disease

Continuously updated · newest added Oct 22, 2026

253 positions on this site are linked to Coronary Artery Disease, out of 107,012 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 Coronary Artery Disease

Sensitive

3-Indolepropionic acid levels in coronary artery disease

ACSM5 · rs6497488

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Sensitive

Hypoxanthine levels in coronary artery disease

LINC02267 · rs117445861

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Sensitive

Coronary artery disease

BCAS3 · rs7214227

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Sensitive

Coronary artery disease

VAMP8 · rs1058588

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Sensitive

Coronary artery disease

near FOXC1 · rs72836800

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Sensitive

Coronary artery disease

GUCY1A3 · rs34914832

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Sensitive

Coronary artery disease

TBX20 · rs2215614

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Sensitive

Psoriasis or coronary artery disease

C19orf38 · rs12979495

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Sensitive

Coronary artery disease

MIA3 · rs3008629

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Sensitive

Coronary artery disease

near FTLP1 · rs8124182

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Sensitive

L-Histidine to Uric acid ratio in coronary artery disease

near RHPN1 · rs73365860

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Sensitive

COVID-19 or coronary artery disease (pleiotropy)

near PARTICL · rs6705971

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Sensitive

Coronary artery disease

CHRNB4 · rs62010554

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Sensitive

Coronary artery disease

DENND2B · rs56210063

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Sensitive

Coronary artery disease

PHB · rs7502499

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Sensitive

Coronary artery disease

near RPL30P9 · rs66778572

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Sensitive

Coronary artery disease

near SLC2A12 · rs2492304

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Sensitive

Coronary artery disease

LPA · rs192425087

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Sensitive

Coronary artery disease

TRPA1 · rs12541758

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Sensitive

Coronary artery disease

FLT1 · rs17086617

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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.