Variants linked to Coronary Artery Disease

Continuously updated · newest added Oct 22, 2026

256 positions on this site are linked to Coronary Artery Disease, out of 107,180 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

ZHX3 · rs6102343

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Sensitive

Coronary atherosclerosis (PheCode 411.4)

near RNU6-758P · rs4888372

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Sensitive

Coronary artery disease

GUCY1A1 · rs3796587

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Sensitive

Coronary artery disease

SMG6 · rs4790881

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Sensitive

Takes medication for coronary artery/ coronary heart disease?

MRPS6 · rs9980618

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Sensitive

L-Tryptophan to 3-Indolepropionic acid ratio in coronary artery disease

ACSM2B · rs73530508

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Sensitive

Coronary artery disease (MTAG)

RYK · rs35432681

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Sensitive

Coronary artery disease (MTAG)

near TBC1D1 · rs1565115

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Sensitive

Coronary artery disease (MTAG)

ZNF827 · rs10006310

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Sensitive

Coronary artery disease (MTAG)

SLC27A6 · rs6865322

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Sensitive

Coronary artery disease (MTAG)

ARHGAP26 · rs3776307

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Sensitive

Coronary artery disease (MTAG)

near EXD1 · rs3959554

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Sensitive

Coronary artery disease and triglyceride levels (multivariate analysis)

FBRSL1 · rs12423664

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Sensitive

Coronary artery disease and LDL cholesterol levels (multivariate analysis)

near BNC2 · rs7033354

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Sensitive

Coronary artery disease

THSD7A · rs17165136

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Sensitive

Coronary artery disease

DAB1 · rs852787

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Sensitive

Coronary artery disease

POM121L9P · rs5760293

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Sensitive

Coronary artery disease

SMAD3 · rs56062135

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Sensitive

Coronary artery disease

near DYM · rs833509

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Sensitive

Coronary artery disease

NCOA6 · rs6088590

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Showing 20 of 256 · page 7 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.