Variants linked to Coronary Artery Disease

Continuously updated · newest added Oct 22, 2026

252 positions on this site are linked to Coronary Artery Disease, out of 106,676 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

Plasma proprotein convertase subtilisin/kexin type 9 levels in stable coronary artery disease

FBXL18 · rs6957201

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Sensitive

Coronary artery disease

ZKSCAN1 · rs6953441

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Sensitive

Coronary artery disease

AKAP13 · rs7177107

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Sensitive

Coronary artery disease

TBL1X · rs5934659

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Sensitive

Coronary artery disease

TIMP2 · rs8075861

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Sensitive

Coronary artery disease

ARL15 · rs7719168

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Sensitive

Coronary artery disease

NGF-AS1 · rs61797068

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Sensitive

Coronary artery disease

near WIPI1 · rs2909217

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Sensitive

Coronary artery disease

UNC13D · rs2410859

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Sensitive

Coronary artery disease

B4GALNT2 · rs191896574

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Sensitive

Coronary artery disease

CABIN1 · rs12484557

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Sensitive

Coronary artery disease

LDAH · rs11124924

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Sensitive

Coronary artery disease

near SNRPEP3 · rs10852238

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Sensitive

Coronary artery disease

FLT1 · rs9513116

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Sensitive

Coronary artery disease

LPA · rs79018195

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Sensitive

Coronary artery disease

CDKN2B-AS1 · rs76959412

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Sensitive

Coronary artery disease

ANKRD55 · rs62362364

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Sensitive

Coronary artery disease

SPECC1L · rs6004124

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Sensitive

Coronary artery disease

SPECC1L-ADORA2A · rs5760309

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Sensitive

Coronary artery disease

near HNRNPKP2 · rs4954580

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Showing 20 of 252 · page 1 of 13

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.