Variants linked to Venous Thromboembolism

Continuously updated · newest added Oct 25, 2026

82 positions on this site are linked to Venous Thromboembolism, out of 117,958 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

Venous thromboembolism

ABO · rs9411377

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Sensitive

Venous thromboembolism

MIR548H5 · rs72983636

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Sensitive

Venous thromboembolism

NME7 · rs16861990

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Sensitive

Venous thromboembolism

MTND1P3 · rs145241704

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Sensitive

Venous thromboembolism

NRG3 · rs1649936

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Sensitive

Venous thromboembolism

FGA · rs6825454

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Sensitive

Venous thromboembolism

KIF26B · rs1756912

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Sensitive

Venous thromboembolism

PSG8 · rs59559305

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Sensitive

Venous thromboembolism

BTNL2 · rs17202393

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Sensitive

Venous thromboembolism adjusted for sickle cell variant rs77121243-T

LOC100130298 · rs142143628

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Sensitive

Venous thromboembolism adjusted for sickle cell variant rs77121243-T

LEMD3 · rs138916004

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Sensitive

Venous thromboembolism adjusted for sickle cell variant rs77121243-T

LY86 · rs3804476

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Sensitive

Venous thromboembolism

F2 · rs1799963

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Sensitive

Venous thromboembolism

F2 · rs3136516

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Sensitive

Venous thromboembolism

ABO · rs2519093

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Sensitive

Venous thromboembolism

THBD · rs1998081

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Sensitive

Venous thromboembolism

F11 · rs4253399

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Standard

Anticoagulant levels

PROCR · rs867186

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Standard

Fibrinogen

FGG · rs7681423

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Sensitive

Venous thromboembolism

F11 · rs3756008

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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.