We identified 12 suitable SNPs with reported associations with dyslexia relatedphenotypes that have the potential to affect local expression levels:rs934634-CYP19A1, rs10046-CYP19A1 andrs555879-MYO5B are located in the 3’-UTR, rs3743205-DYX1C1, rs2038137-KIAA0319 andrs3178-NRSN1 are located in the 5’-UTR.Rs600753-DYX1C1, rs17819126-DYX1C1,rs9467075-DCDC2, rs3734972-FLNC andrs4504469-KIAA0319 are exonic SNPs, andrs2143340-TDP2 is located in a non-coding exon. The gene discussed is NRSN1; the disease is dyslexia.