ADHDgene Database

SNP Report

Basic Info

Name	rs5568 dbSNP Ensembl
Location	Chr16:55730124(Fwd)
Variant Alleles	A/C
Ancestral Allele	A
Functional Annotation	downstream_gene_variant; intron_variant; upstream_gene_variant.
Consequence to Transcript	downstream_gene_variant(ENST00000568529) intron_variant(ENST00000414754; ENST00000567238; ENST00000566163; ENST00000568943; ENST00000219833; ENST00000561820; ENST00000379906) upstream_gene_variant(ENST00000574918)
No. of Studies	2 (significant: 0; non-significant: 2; trend: 0)
Source	Literature-origin

SNP related studies (count: 2)

Reference	Allele Change	Risk Allele	Statistical Values	Author Comments	Result of Statistical Analysis
Kim JW, 2008			X²=0.04, P-value=0.84, OR=1.02 X²=0.04, P-value=0.84, OR=1.02	not associated with ADHD not associated with ADHD	Non-significant
Hawi, Z., 2012	A:C	C	P-value=0.3708, X²=0.8, OR=1.13, 95% CI=0.86-1.48 P-value=0.3708, X²=0.8, OR=1.13, 95% CI=0.86-1.48	The marker did not show significant association with ADHD. The marker did not show significant association with ADHD.	Non-significant

SNP related genes (count: 2)

Approved Symbol	Approved Name	Location	No. of Studies (significant/non-significant/trend)
SLC6A2	solute carrier family 6 (neurotransmitter transporter, noradrenalin), member 2	16q12.2	16(10/5/1)
NET1	neuroepithelial cell transforming 1	10p15	0

SNPs in LD with rs5568 (count: 1) View in gBrowse (chr16:55730124..55731575 )

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