Variants linked to Schizophrenia

Continuously updated · newest added Oct 24, 2026

212 positions on this site are linked to Schizophrenia, out of 113,826 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 Schizophrenia

Sensitive

Biological Mother: Schizophrenia

near LINC01673 · rs192439018

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Sensitive

Bipolar disorder lithium response (categorical) or schizophrenia

ADAMTSL3 · rs66486766

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Sensitive

Biological Father: Schizophrenia

near UBE3D · rs115632032

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Sensitive

Biological Father: Schizophrenia

PLCB1 · rs373182523

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Sensitive

Biological Father: Schizophrenia

ITSN2 · rs188839242

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Sensitive

Autism spectrum disorder or schizophrenia

HLA-DRB1 · rs184153866

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Sensitive

Plasma norclozapine levels in treatment-resistant schizophrenia

UGT2B10 · rs11725502

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Sensitive

Autism spectrum disorder or schizophrenia

HLA-DRA · rs9269271

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Sensitive

Biological Grandparent (maternal): Schizophrenia

near LINC02379 · rs75381199

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Sensitive

Schizophrenia or ER positive breast cancer (pleiotropy)

near HCN1 · rs7447717

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Sensitive

Autism spectrum disorder or schizophrenia

ABHD16A · rs707939

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Sensitive

Schizophrenia or ER positive breast cancer (pleiotropy)

near MAPK8IP1P1 · rs2532363

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Sensitive

Autism spectrum disorder or schizophrenia

HIST1H1B · rs202906

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Sensitive

Schizophrenia or breast cancer (pleiotropy)

near GATAD2A · rs2905432

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Sensitive

Clozapine-to-N-desmethylclozapine metabolic ratio in schizophrenia

CTD-2005D20.1 · rs10023464

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Sensitive

Autism spectrum disorder or schizophrenia

GPX5 · rs141342723

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Sensitive

Neutrophil level response to clozapine in treatment-resistant schizophrenia

ZNF618 · rs77198048

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Sensitive

Broad depression or schizophrenia

SPATA31D1 · rs2026194

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Sensitive

Broad depression or schizophrenia

STK19 · rs389883

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Sensitive

Broad depression or schizophrenia

MATN1 · rs12407717

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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.