ADHDgene Database

SNP Report

Basic Info

Name	rs1387926 dbSNP Ensembl
Location	chr9:87632663(Fwd)
Variant Alleles	C/T
Ancestral Allele	C
Functional Annotation	intron_variant.
Consequence to Transcript	intron_variant(ENST00000277120; ENST00000323115; ENST00000376213; ENST00000376214)
No. of Studies	1 (significant: 1; non-significant: 0; trend: 0)
Source	Literature-origin

SNP related studies (count: 1)

Reference	Allele Change	Risk Allele	Statistical Values	Author Comments	Result of Statistical Analysis
Ribases M, 2008			genotypic P-value=8e-04; genotypic P-value=0.0011, OR=1.75 (...... genotypic P-value=8e-04; genotypic P-value=0.0011, OR=1.75 (1.23-2.44) in dominant model; genotypic P-value=0.012, OR=7.14 (.96-50) in recessive model; allelic P-value=3.6e-04, OR=1.75 (1.27-2.4) in Children More...	provided evidence of association with childhood ADHD provided evidence of association with childhood ADHD	Significant

SNP related genes (count: 1)

Approved Symbol	Approved Name	Location	No. of Studies (significant/non-significant/trend)
NTRK2	neurotrophic tyrosine kinase, receptor, type 2	9q22.1	1(1/0/0)

SNPs in LD with rs1387926 (count: 24) View in gBrowse (chr9:87576842..87686259 )

The LD data used here is based on HapMap rel#27. LD SNP pairs were selected with a threshold r²>=0.8.