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rare copy number variants risk_factor_for schizophrenia

Subject
rare copy number variants
Relation
risk_factor_for
Object
schizophrenia
p-value
Evidence from: primary | all sources

Evidence (1 sources)

Mapping genomic loci implicates genes and synaptic biology in schizophrenia. (2022) PMID:35396580 cited
rare copy number variants (CNVs) ... are genetic ... variation in risk ... associated with schizophrenia
confidence: 0.95