Variants linked to Substance Use Disorder

Continuously updated · newest added Sep 30, 2026

206 positions on this site are linked to Substance Use Disorder, out of 25,192 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 Substance Use Disorder

Sensitive

Substance use disorder

OPRD1 · rs2236860

See detailed info →
Sensitive

Substance use disorder

PDE4B · rs4503327

See detailed info →
Sensitive

Substance use disorder

PDE4B · rs12729364

See detailed info →
Sensitive

Substance use disorder

PDE4B · rs7519259

See detailed info →
Sensitive

Substance use disorder

PDE4B · rs4655601

See detailed info →
Sensitive

Substance use disorder

PDE4B · rs1084490

See detailed info →
Sensitive

Substance use disorder

DPYD · rs11165875

See detailed info →
Sensitive

Substance use disorder

DPYD · rs4950035

See detailed info →
Sensitive

Substance use disorder

RABGAP1L · rs1653636

See detailed info →
Sensitive

Substance use disorder

CDC42BPA · rs7556248

See detailed info →
Sensitive

Substance use disorder

GTF3C2 · rs3739095

See detailed info →
Sensitive

Substance use disorder

near CCDC85A · rs4624427

See detailed info →
Sensitive

Substance use disorder

THSD7B · rs352181

See detailed info →
Sensitive

Substance use disorder

ARHGAP15 · rs4233566

See detailed info →
Sensitive

Substance use disorder

near TANK · rs17287470

See detailed info →
Sensitive

Substance use disorder

near TANK · rs76834425

See detailed info →
Sensitive

Substance use disorder

near SPATS2L · rs4673905

See detailed info →
Sensitive

Substance use disorder

near CREB1 · rs13392734

See detailed info →
Sensitive

Substance use disorder

near DAZL · rs7617386

See detailed info →
Sensitive

Substance use disorder

SRRM3 · rs6956241

See detailed info →

Showing 20 of 206 · page 1 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.