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

SEC31A · rs6826579

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Sensitive

Venous thromboembolism

MS4A4A · rs55777218

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Sensitive

Venous thromboembolism

C1orf198 · rs145470028

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Sensitive

Venous thromboembolism

IGFBP3 · rs73692310

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Sensitive

Venous thromboembolism

SOX6 · rs12800654

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Sensitive

Venous thromboembolism

near Y_RNA · rs115924439

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Sensitive

Venous thromboembolism recurrence in VTE

near SPMAP2L · rs28752105

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Sensitive

Venous thromboembolism recurrence in deep vein thrombosis as first VTE

near RNA5SP441 · rs117366080

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Sensitive

Venous thromboembolism

ZBTB16 · rs1997547

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Sensitive

Venous thromboembolism

FUNDC2 · rs17328181

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Sensitive

Venous thromboembolism recurrence in provoked as first VTE

ZNF423 · rs112440311

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Sensitive

Venous thromboembolism

STX10 · rs7508633

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Sensitive

Venous thromboembolism recurrence in pulmonary embolism as first VTE

STXBP5L · rs148458707

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Sensitive

Venous thromboembolism

SCARA5 · rs10087301

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Sensitive

Venous thromboembolism recurrence in unprovoked as first VTE

LINC01924 · rs148611543

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Sensitive

Venous thromboembolism

F7 · rs568849616

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Sensitive

Venous thromboembolism recurrence in provoked as first VTE

near ARL17B · rs3744462

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Sensitive

Venous thromboembolism recurrence in VTE

near LINC03000 · rs145765113

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Sensitive

Venous thromboembolism recurrence in pulmonary embolism as first VTE

SLC4A1 · rs45562031

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Sensitive

Venous thromboembolism recurrence in provoked as first VTE

PRKG1 · rs113846542

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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.