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 25,445 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

near NEGR1 · rs4650105

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Sensitive

Substance use disorder

near SIX3 · rs472140

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Sensitive

Substance use disorder

near PDCL3 · rs4851350

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Sensitive

Substance use disorder

near ZEB2 · rs79106351

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Sensitive

Substance use disorder

SPATS2L · rs6743157

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Sensitive

Substance use disorder

ERC2 · rs12496267

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Sensitive

Substance use disorder

ERC2 · rs2316482

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Sensitive

Substance use disorder

ERC2 · rs71309948

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Sensitive

Substance use disorder

near GBE1 · rs58586881

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Sensitive

Substance use disorder

GBE1 · rs7631349

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Sensitive

Substance use disorder

near GBE1 · rs2315967

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Sensitive

Substance use disorder

ST3GAL6 · rs9811449

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Sensitive

Substance use disorder

ZBTB20 · rs78512230

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Sensitive

Substance use disorder

ZIC1 · rs73004652

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Sensitive

Substance use disorder

near RSRC1 · rs2956471

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Sensitive

Substance use disorder

BANK1 · rs13129744

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Sensitive

Substance use disorder

BANK1 · rs13119516

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Sensitive

Substance use disorder

SLC39A8 · rs34333163

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Sensitive

Substance use disorder

INPP4B · rs331951

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Sensitive

Substance use disorder

near INPP4B · rs72717312

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Showing 20 of 206 · page 6 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.