Fig. 1From: Identification of deleterious and regulatory genomic variations in known asthma lociNumber of asthma-associated variants by annotation. Genomic variants were previously reported by genome-wide association or candidate gene studies of asthma and asthma related traits. Annotations derived from SnpEff indicate that approximately 12% of the known asthma variants code for a missense or non-sense variant, whereas the majority are non-coding or have no known functionBack to article page