Genomic sequencing of a dyslexia susceptibility haplotype encompassing ROBO1

Table 2 SNVs in ROBO1 and 1-Mb upstream region on two samples from CGI and Illumina pooled samples

Genomic function	Shared variants^a	Shared heterozygotes	Novel SNVs^b
Exonic	0	0	0
Intronic	597	290	1
5′UTR	1	0	0
Upstream (1 Mb)	852	374	3

^aVariants showing in both Illumina pooled samples and two CGI individual samples
^bNot annotated in dbSNP version 137

ISSN: 1866-1955