Variants linked to Schizophrenia

Continuously updated · newest added Oct 24, 2026

212 positions on this site are linked to Schizophrenia, out of 113,994 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

Schizophrenia

SUMO2P1 · rs138488080

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Sensitive

Schizophrenia

NOTCH4 · rs115344853

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Sensitive

Schizophrenia

DDR1 · rs116396069

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Sensitive

Schizophrenia

PSORS1C1 · rs149979052

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Sensitive

Schizophrenia

DPCR1 · rs115123027

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Sensitive

Schizophrenia

HLA-X · rs114618162

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Sensitive

Schizophrenia

ZNF311 · rs116757206

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Sensitive

Schizophrenia

ZKSCAN4 · rs17720293

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Sensitive

Schizophrenia

TRIM27 · rs182812355

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Sensitive

Schizophrenia

OR12D3 · rs114071887

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Sensitive

Schizophrenia

RERE · rs172531

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Sensitive

Schizophrenia

LOC10050743 · rs10791098

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Sensitive

Schizophrenia

LOC10050547 · rs715170

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Sensitive

Schizophrenia

HIST1H3D · rs67575965

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Sensitive

Schizophrenia

OR2B8P · rs202904

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Sensitive

Schizophrenia

LOC10050653 · rs35225048

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Sensitive

Schizophrenia

ADAM10 · rs12911832

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Sensitive

Schizophrenia

TMTC1 · rs302321

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Sensitive

Schizophrenia

LOC10013250 · rs28758902

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Sensitive

Schizophrenia

UBE2Q2P1 · rs12902973

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Showing 20 of 212 · 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.