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 25,501 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 · rs1989903

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Sensitive

Substance use disorder

CNOT4 · rs11772832

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Sensitive

Substance use disorder

near VAX1 · rs73385301

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Sensitive

Substance use disorder

METTL15 · rs11030330

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Sensitive

Substance use disorder

CEP57 · rs56298021

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Sensitive

Substance use disorder

DRD2 · rs7122246

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Sensitive

Substance use disorder

near TMPRSS5 · rs112991785

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Sensitive

Substance use disorder

TMPRSS5 · rs7110736

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Sensitive

Substance use disorder

near USP28 · rs61907877

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Sensitive

Substance use disorder

HTR3A · rs61905785

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Sensitive

Substance use disorder

NTM · rs7942876

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Sensitive

Substance use disorder

near NTM · rs4937696

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Sensitive

Substance use disorder

SEMA6D · rs281280

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Sensitive

Substance use disorder

near BNC1 · rs35563832

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Sensitive

Substance use disorder

ZCCHC14 · rs3748400

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Sensitive

Substance use disorder

RAB27B · rs11151976

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Sensitive

Substance use disorder

MAU2 · rs12463074

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Sensitive

Substance use disorder

near RNF114 · rs7272308

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Sensitive

Substance use disorder

TCF20 · rs9306356

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Sensitive

Substance use disorder

SZT2 · rs2842179

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Showing 20 of 206 · page 8 of 11

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.