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 25,361 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

near ZEB2 · rs1346344

See detailed info →
Sensitive

Substance use disorder

BSN · rs9836291

See detailed info →
Sensitive

Substance use disorder

CADM2 · rs7644873

See detailed info →
Sensitive

Substance use disorder

RSRC1 · rs7629432

See detailed info →
Sensitive

Substance use disorder

near GATB · rs6812000

See detailed info →
Sensitive

Substance use disorder

RANBP17 · rs4286697

See detailed info →
Sensitive

Substance use disorder

near POM121L2 · rs9461366

See detailed info →
Sensitive

Substance use disorder

near ZNF391 · rs34953377

See detailed info →
Sensitive

Substance use disorder

near SCAND3 · rs34470113

See detailed info →
Sensitive

Substance use disorder

near TRIM27 · rs417919

See detailed info →
Sensitive

Substance use disorder

near OR2J2 · rs9257572

See detailed info →
Sensitive

Substance use disorder

TMEM120A · rs10954732

See detailed info →
Sensitive

Substance use disorder

near LONRF1 · rs7812870

See detailed info →
Sensitive

Substance use disorder

SLC7A13 · rs2954344

See detailed info →
Sensitive

Substance use disorder

RUNX1T1 · rs9297901

See detailed info →
Sensitive

Substance use disorder

near VEGFB · rs57831436

See detailed info →
Sensitive

Substance use disorder

RPS6KA4 · rs72924202

See detailed info →
Sensitive

Substance use disorder

near RPS6KA4 · rs11231787

See detailed info →
Sensitive

Substance use disorder

NCAM1 · rs7129926

See detailed info →
Sensitive

Substance use disorder

DRD2 · rs75644434

See detailed info →

Showing 20 of 206 · page 4 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.