ADHDgene Database

SNP Report

Basic Info

Name	rs6884105 dbSNP Ensembl
Location	Chr5:159348443(Fwd)
Variant Alleles	G/A
Ancestral Allele	A
Functional Annotation	intron_variant.
Consequence to Transcript	intron_variant(ENST00000306675)
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	G:A	G	P-value=0.3819, X²=0.77, OR=1.13, 95% CI=0.86-1.4...... P-value=0.3819, X²=0.77, OR=1.13, 95% CI=0.86-1.46 More...	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)
ADRA1B	adrenergic, alpha-1B-, receptor	5q33.3	2(1/1/0)

SNPs in LD with rs6884105 (count: 4) View in gBrowse (chr5:159339533..159369429 )

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

rs_ID	Functional Annotation	#studies(significant/non-significant/trend)	r²[population]

rs7737796	intron_variant	1(1/0/0)	0.875[JPT]
rs6892282	intron_variant	1(0/1/0)	0.88[JPT]

rs_ID	Functional Annotation	r²[population]
rs1019920	upstream_gene_variant	0.96[CEU]; 0.93[CHB]; 0.831[YRI]
rs11952941	intron_variant	0.801[CHB]; 0.88[JPT]