ADHDgene Database

SNP Report

Basic Info

Name	rs3808585 dbSNP Ensembl
Location	Chr8:26724326(Fwd)
Variant Alleles	C/T
Ancestral Allele	C
Functional Annotation	intron_variant; upstream_gene_variant.
Consequence to Transcript	intron_variant(ENST00000380573) upstream_gene_variant(ENST00000519229; ENST00000519096; ENST00000380582; ENST00000521711; ENST00000380586; ENST00000276393; ENST00000354550; ENST00000380572; ENST00000358857; ENST00000380587; ENST00000380581)
No. of Studies	1 (significant: 0; non-significant: 1; trend: 0)
Source	Literature-origin

SNP related studies (count: 1)

Reference	Allele Change	Risk Allele	Statistical Values	Author Comments	Result of Statistical Analysis
Hawi, Z., 2012	C:T	C	P-value=0.829, X²=0.05, OR=1.03, 95% CI=0.77-1.37 P-value=0.829, X²=0.05, OR=1.03, 95% CI=0.77-1.37	The marker did not show significant association with ADHD. The marker did not show significant association with ADHD.	Non-significant

SNP related genes (count: 1)

Approved Symbol	Approved Name	Location	No. of Studies (significant/non-significant/trend)
ADRA1A	adrenergic, alpha-1A-, receptor	8p21.2	3(2/1/0)

SNPs in LD with rs3808585 (count: 1) View in gBrowse (chr8:26724326..26725568 )

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