Enrichment of putatively damaging rare variants in the DYX2 locus and the reading-related genes CCDC136 and FLNC.

Hum Genet · 2017 · PMC5702371 · PMID 28866788

Europe PMC DOI

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closest p · 1.0× alpha

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nominally significantP < 0.05actually significant

CNTNAP2 , COMT , DBH , DCDC2 - KIAA0319 , DRD2 , DYX1C1 , and FOXP2 had nominally significant results (uncorrected P < 0.05) for multiple SNPs in the CLDRC.

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