ADHDgene Database

SNP Report

Basic Info

Name	rs36017 dbSNP Ensembl
Location	Chr16:55718818(Fwd)
Variant Alleles	G/C
Ancestral Allele	C
Functional Annotation	intron_variant.
Consequence to Transcript	intron_variant(ENST00000568943; ENST00000567238; ENST00000219833; ENST00000566163; ENST00000568529; ENST00000414754; ENST00000379906; ENST00000561820)
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
Sengupta, S. M., 2012	C/G		P-value=0.13, Z statistic (allele 1)=¨C1.53 P-value=0.13, Z statistic (allele 1)=¨C1.53	No significant association was found in this study. No significant association was found in this study.	Non-significant
Hawi, Z., 2012	C:G	G	P-value=0.792, X²=0.07, OR=1.04, 95% CI=0.80-1.33 P-value=0.792, X²=0.07, OR=1.04, 95% CI=0.80-1.33	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)
SLC6A2	solute carrier family 6 (neurotransmitter transporter, noradrenalin), member 2	16q12.2	16(10/5/1)

SNPs in LD with rs36017 (count: 8) View in gBrowse (chr16:55718818..55729124 )

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]

rs2279805	downstream_gene_variant; intron_variant	1(0/1/0)	0.925[CEU]; 0.869[TSI]
rs1345429	intron_variant	1(0/1/0)	0.925[CEU]; 0.875[MEX]; 0.869[TSI]