ADHDgene Database

SNP Report

Basic Info

Name	rs6116268 dbSNP Ensembl
Location	Chr20:4211440(Fwd)
Variant Alleles	T/C
Ancestral Allele	C
Functional Annotation	intron_variant.
Consequence to Transcript	intron_variant(ENST00000379453)
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	T:C	T	P-value=0.61, X²=0.26, OR=1.07, 95% CI=0.83-1.36 P-value=0.61, X²=0.26, OR=1.07, 95% CI=0.83-1.36	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)
ADRA1D	adrenergic, alpha-1D-, receptor	20p13	1(0/1/0)

SNPs in LD with rs6116268 (count: 1) View in gBrowse (chr20:4211440..4215557 )

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]

rs1556832	intron_variant	1(0/1/0)	0.922[CEU]; 0.911[MEX]; 0.865[TSI]