ADHDgene Database

SNP Report

Basic Info

Name	rs550942 dbSNP Ensembl
Location	chr11:58394154(Fwd)
Variant Alleles	C/T
Ancestral Allele	T
Functional Annotation	downstream_gene_variant.
Consequence to Transcript	downstream_gene_variant(ENST00000361987; ENST00000389919; ENST00000422974)
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=0.019; genotypic P-value=0.006, OR=1.64 (1...... genotypic P-value=0.019; genotypic P-value=0.006, OR=1.64 (1.15-2.38) in dominant model; genotypic P-value=0.77 in recessive model; allelic P-value=0.013, OR=1.48 (1.08-2.04) in Adults More...	provided evidence of association with adulthood ADHD provided evidence of association with adulthood ADHD	Significant

SNP related genes (count: 2)

Approved Symbol	Approved Name	Location	No. of Studies (significant/non-significant/trend)
CNTF	ciliary neurotrophic factor	11q12	1(1/0/0)

Approved Symbol	Approved Name	Location
ZFP91-CNTF	ZFP91-CNTF readthrough (NMD candidate)	11q12.1

SNPs in LD with rs550942 (count: 1) View in gBrowse (chr11:58394154..58415508 )

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