Fig. 1
From: A missense variant in SLC39A8 is associated with severe idiopathic scoliosis
Manhattan plot showing AIS exome-wide association results. Linear regression p-values (−log10) for 52,480 single-nucleotide polymorphisms with minor allele frequency > 0.01. One SNP (rs13107325) was significantly associated with AIS after Bonferroni correction for multiple tests
