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 106,844 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

near HNRNPKP2 · rs4954580

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Sensitive

Coronary artery disease

SMG6 · rs2641438

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Sensitive

Coronary artery disease

NR2C1 · rs933899

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Sensitive

Coronary artery disease

TMEM41B · rs4537761

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Sensitive

Coronary artery disease

SMARCA4 · rs3786723

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Sensitive

Coronary artery disease

CXCL12 · rs1746049

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Sensitive

Coronary artery disease

NEDD4 · rs11633313

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Sensitive

Coronary artery disease

FLT1 · rs9513112

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Sensitive

Coronary artery disease

near MLN · rs62397561

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Sensitive

Coronary artery disease

PID1 · rs4140748

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Sensitive

Coronary artery disease

GABBR1 · rs29266

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Sensitive

Coronary artery disease

ITPK1 · rs1956028

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Sensitive

Coronary artery disease

OPHN1 · rs1410127

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Sensitive

Coronary artery disease

FER · rs112949822

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Sensitive

Coronary artery disease

C9orf84 · rs10981012

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Sensitive

Ticagrelor levels in individuals with acute coronary syndromes treated with ticagrelor

STAG3 · rs117038461

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Sensitive

Coronary artery disease

UFL1-AS1 · rs11152953

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Sensitive

Coronary artery disease

DCLK2 · rs9985766

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Sensitive

Coronary artery disease

PAWR · rs8176893

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Sensitive

Coronary artery disease

near NAT2 · rs4646249

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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.