Extended Data Fig. 4: Variant effect predictor summary for the credible set of variants significantly associated with dyslexia.
From: Discovery of 42 genome-wide significant loci associated with dyslexia
Summary information is output from the online variant effect predictor in ENSEMBL (release 104). All our variants were present in the 1000 Genomes reference panel so are considered existing, and no pre-filtering (for example, on MAF; consequence type) was done.
