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Journal of Neurodevelopmental Disorders
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Table 2 SNVs in
ROBO1
and 1-Mb upstream region on two samples from CGI and Illumina pooled samples
From:
Genomic sequencing of a dyslexia susceptibility haplotype encompassing
ROBO1
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
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