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Copy number variation (CNV) risk_factor_for psychiatric disorders

Subject
Copy number variation (CNV)
Relation
risk_factor_for
Object
psychiatric disorders
p-value
Evidence from: primary | all sources

Evidence (1 sources)

CNVs: harbingers of a rare variant revolution in psychiatric genetics. (2012) PMID:22424231 cited
rare CNV alleles in psychiatric disease ... conferring significant disease risks
confidence: 0.95