ADHDgene Database

SNP Report

Basic Info

Name	rs10780695 dbSNP Ensembl
Location	Chr9:87644233(Fwd)
Variant Alleles	T/C
Ancestral Allele	T
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=0.067; genotypic P-value=0.083 in dominant...... genotypic P-value=0.067; genotypic P-value=0.083 in dominant model; genotypic P-value=0.048, OR=1.78 (1.02-1.61) in recessive model; allelic P-value=0.03, OR=1.28 (1.02-1.59) 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 rs10780695 (count: 10) View in gBrowse (chr9:87644233..87682475 )

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