COMT Met allele risk_factor_for autism spectrum disorder

Subject: COMT Met allele
Relation: risk_factor_for
Object: autism spectrum disorder
p-value: —

Evidence from: primary | all sources

Evidence (1 sources)

Multiple recurrent de novo CNVs, including duplications of the 7q11.23 Williams syndrome region, are strongly associated with autism. (2011) PMID:21658581 cited

the MET oncogene ... recent common variant findings

confidence: 0.85