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

UBE2Q2P1 · rs12902973

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Sensitive

Schizophrenia

LRRC16A · rs6918354

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Sensitive

Schizophrenia

TOMM22P6 · rs6804239

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Sensitive

Schizophrenia

HLA-DOB · rs114377514

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Sensitive

Schizophrenia

DLG2 · rs1864774

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Sensitive

Schizophrenia

TTC12 · rs4987094

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Sensitive

Schizophrenia

C10orf32-AS · rs11191424

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Sensitive

Schizophrenia

PRDM14 · rs7012816

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Sensitive

Schizophrenia

LOC10013228 · rs16880831

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Sensitive

Schizophrenia

LOC10042066 · rs12619354

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Sensitive

Schizophrenia

LOC645314 · rs10204454

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Sensitive

Schizophrenia

EPC2 · rs12622667

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Sensitive

Autism spectrum disorder or schizophrenia

HCG4B · rs111312615

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Sensitive

Autism spectrum disorder or schizophrenia

GPX5 · rs6921919

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Sensitive

Autism spectrum disorder or schizophrenia

ABHD16A · rs115035678

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Sensitive

Autism spectrum disorder or schizophrenia

HLA-DRB1 · rs142972412

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Sensitive

Autism spectrum disorder or schizophrenia

HCG14 · rs115661163

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Sensitive

Autism spectrum disorder or schizophrenia

HFE · rs61472021

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Sensitive

Autism spectrum disorder or schizophrenia

ABCF1 · rs115242751

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Sensitive

Schizophrenia

SPATS2L · rs17630293

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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.