Variants linked to Adventurousness

Continuously updated · newest added Oct 11, 2026

152 positions on this site are linked to Adventurousness, out of 64,299 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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Standard

Automobile speeding propensity

CADM2 · rs17516256

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Standard

Smoking status (ever vs never smokers)

NT5C2 · rs7092200

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Standard

Smoking status (ever vs never smokers)

REV3L · rs240955

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General risk tolerance (MTAG)

XKR6 · rs4841503

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Number of sexual partners

METTL15 · rs16918024

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Adventurousness

BHLHE22 · rs62519839

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Standard

Adventurousness

IRX3 · rs17260689

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Risk-taking tendency (4-domain principal component model)

TMEM180 · rs11592299

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Standard

Adventurousness

CD34 · rs984983

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Adventurousness

PCDH7 · rs73219118

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Standard

Smoking status (ever vs never smokers)

CA10 · rs2202237

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Standard

General risk tolerance (MTAG)

ZBTB20 · rs116493405

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Standard

Smoking status (ever vs never smokers)

TRIM8 · rs12764388

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Standard

Smoking status (ever vs never smokers)

RUNX1T1 · rs13258512

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Standard

Adventurousness

LRFN2 · rs75108536

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Standard

Automobile speeding propensity

FOXP1 · rs11128203

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Standard

Smoking status (ever vs never smokers)

FOXG1 · rs11844846

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Standard

Smoking status (ever vs never smokers)

CADM2 · rs117898875

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Standard

Smoking status (ever vs never smokers)

PTBP2 · rs553785

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Standard

Smoking status (ever vs never smokers)

OPCML · rs78058594

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Showing 20 of 152 · page 1 of 8

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.