ADHDgene Database

SNP Report

Basic Info

Name	rs1080750 dbSNP Ensembl
Location	Chr9:34581525(Fwd)
Variant Alleles	C/T
Ancestral Allele	C
Functional Annotation	intron_variant; nc_transcript_variant.
Consequence to Transcript	intron_variant(ENST00000378980; ENST00000351266; ENST00000438244; ENST00000453642; ENST00000417345; ENST00000436360) nc_transcript_variant(ENST00000438244; ENST00000453642; ENST00000436360)
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=0.12; genotypic P-value=0.14 in dominant m...... genotypic P-value=0.12; genotypic P-value=0.14 in dominant model; genotypic P-value=0.063 in recessive model; allelic P-value=0.048, OR=1.23 (1-1.51) 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)
CNTFR	ciliary neurotrophic factor receptor	9p13	1(1/0/0)

SNPs in LD with rs1080750 (count: 1) View in gBrowse (chr9:34581525..34669005 )

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