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

Coronary artery disease

near MIR548G · rs6810798

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Sensitive

Coronary artery disease

PPAP2B · rs147055617

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Sensitive

Coronary artery disease

near PRIM2 · rs11752218

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Sensitive

Coronary artery disease

STN1 · rs2067831

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Sensitive

Coronary artery disease (MTAG)

near LINC02881 · rs1746050

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Sensitive

Coronary artery disease

TEX41 · rs10928241

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Sensitive

Eudesmic acid (3,4,5-trimethoxybenzoic acid) levels in coronary artery disease

EDNRB-AS1 · rs9530695

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Sensitive

Coronary artery disease

near CRIPTO3 · rs7884019

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Sensitive

Coronary artery disease

CNNM2 · rs77787671

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Sensitive

Coronary artery disease

near PLG · rs28867400

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Sensitive

Coronary artery disease (MTAG)

CDKN2A · rs3731239

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Sensitive

Coronary artery disease

COL4A2 · rs7333991

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Sensitive

Psoriasis or coronary artery disease

near COQ10A · rs76151170

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Sensitive

Coronary artery disease

near PRMT5P1 · rs17612693

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Sensitive

2-Methylsuccinic acid levels in coronary artery disease

ACADS · rs9204

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Sensitive

Coronary artery disease

MORF4L1 · rs11637783

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Sensitive

Coronary artery disease

MIA3 · rs17163363

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Sensitive

Coronary artery disease

near IGF2R · rs6932293

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Sensitive

Coronary artery disease

WDR12 · rs148812085

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Sensitive

Coronary artery disease

PHACTR1 · rs9381634

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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.