ADHDgene Database

SNP Report

Basic Info

Name	rs3785155 dbSNP Ensembl
Location	Chr16:55722390(Fwd)
Variant Alleles	G/A
Ancestral Allele	G
Functional Annotation	intron_variant.
Consequence to Transcript	intron_variant(ENST00000566163; ENST00000414754; ENST00000219833; ENST00000379906; ENST00000568529; ENST00000567238; ENST00000568943; ENST00000561820)
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
Sengupta, S. M., 2012	G/A		P-value=0.98, Z statistic (allele 1)=0.03 P-value=0.98, Z statistic (allele 1)=0.03	No significant association was found in this study. No significant association was found in this study.	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 rs3785155 (count: 5) View in gBrowse (chr16:55717483..55724439 )

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]
rs10521329	intron_variant	2(0/2/0)	0.824[MEX]; 0.805[TSI]