Variants linked to Venous Thromboembolism

Continuously updated · newest added Oct 25, 2026

82 positions on this site are linked to Venous Thromboembolism, out of 117,874 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 Venous Thromboembolism

Sensitive

Deep vein thrombosis [DVT] (PheCode 452.2)

TC2N · rs58763793

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Sensitive

Venous thromboembolism

near LINC03125 · rs35073727

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Sensitive

Deep vein thrombosis [DVT] (PheCode 452.2)

VWF · rs4764533

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Sensitive

Venous thromboembolism

SCARA5 · rs2726950

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Sensitive

Venous thromboembolism

LRP4 · rs191945075

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Sensitive

Venous thromboembolism

RORA · rs340009

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Sensitive

Venous thromboembolism

ACAD10 · rs56750693

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Sensitive

Venous thromboembolism

F5 · rs4524

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Sensitive

Venous thromboembolism

MECOM · rs7613621

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Sensitive

Venous thromboembolism

LNPEP · rs38032

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Sensitive

Venous thromboembolism

near OR5AK3P · rs141687379

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Sensitive

Venous thromboembolism

KIRREL3 · rs35257264

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Sensitive

Venous thromboembolism

VWF · rs1558519

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Sensitive

Venous thromboembolism

PLCG2 · rs56943275

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Sensitive

Venous thromboembolism

near CD93 · rs79388863

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Sensitive

Venous thromboembolism

PROCR · rs6060288

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Sensitive

Venous thromboembolism

near SPSB1 · rs9442571

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Sensitive

Venous thromboembolism

AK5 · rs12753797

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Sensitive

Venous thromboembolism

PROC · rs1158867

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Sensitive

Venous thromboembolism

ARL13B · rs28479320

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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.