rare CNV risk_factor_for autism

Subject: rare CNV
Relation: risk_factor_for
Object: autism
p-value: —

Evidence from: primary | all sources

Evidence (1 sources)

Genome-wide analysis of copy number variants in attention deficit hyperactivity disorder: the role of rare variants and duplications at 15q13.3. (2012) PMID:22420048 cited

did not report perfect cosegregation of risk variants with ADHD (16, 39) or autism (40)

confidence: 0.90