A regional burden of sequence-level variation in the 22q11.2 region influences schizophrenia risk and educational attainment

Genomic loci where recurrent pathogenic CNVs are associated with psychiatric phenotypes in the population may also be sensitive to the collective impact of multiple functional low-frequency single nucleotide variants (SNVs).

Go to Source

This article was first shared by INDoximity

You may also like...

Enable Notifications    OK No thanks