Variants linked to Substance Use Disorder

Continuously updated · newest added Oct 1, 2026

206 positions on this site are linked to Substance Use Disorder, out of 25,235 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

Substance use disorder

FOXP2 · rs2189010

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Sensitive

Substance use disorder

CNOT4 · rs2718167

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Sensitive

Substance use disorder

XPO7 · rs66824050

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Sensitive

Substance use disorder

RUNX1T1 · rs4735044

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Sensitive

Substance use disorder

CSMD3 · rs6469450

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Sensitive

Substance use disorder

near PTK2 · rs55793749

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Sensitive

Substance use disorder

near CCDC171 · rs141443468

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Sensitive

Substance use disorder

near GAPVD1 · rs3104553

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Sensitive

Substance use disorder

PRRC2B · rs182293592

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Sensitive

Substance use disorder

near BRD3 · rs55931012

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Sensitive

Substance use disorder

near CELF2 · rs10508408

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Sensitive

Substance use disorder

near LDB1 · rs12768433

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Sensitive

Substance use disorder

near ELOVL3 · rs12773990

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Sensitive

Substance use disorder

NFKB2 · rs11574851

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Sensitive

Substance use disorder

near TRIM8 · rs12765060

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Sensitive

Substance use disorder

near METTL15 · rs2582894

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Sensitive

Substance use disorder

near TMPRSS5 · rs7123334

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Sensitive

Substance use disorder

near TMPRSS5 · rs73004043

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Sensitive

Substance use disorder

near TMPRSS5 · rs12281062

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Sensitive

Substance use disorder

ZBTB16 · rs238910

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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.