ADHDgene Database

SNP Report

Basic Info

Name	rs9929758 dbSNP Ensembl
Location	Chr16:84430781(Fwd)
Variant Alleles	T/C
Ancestral Allele	T
Functional Annotation	intron_variant.
Consequence to Transcript	intron_variant(ENST00000262429; ENST00000416219)
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
Hinney, A., 2011		T	GWAS P-value=5.47E-05, OR=1.57, Replication FBAT P-value=0.5...... GWAS P-value=5.47E-05, OR=1.57, Replication FBAT P-value=0.5485, Combination P-value=9.60E-05 More...	This GWAS in a small group of clinically ascertained young G...... This GWAS in a small group of clinically ascertained young German patients with ADHD and population-based controls did not reveal genome-wide significant findings. Replication attempts in further German and international samples did also not lead to a P-value(s) below 5E-08. More...	Non-significant

SNP related genes (count: 1)

Approved Symbol	Approved Name	Location	No. of Studies (significant/non-significant/trend)
ATP2C2	ATPase, Ca++ transporting, type 2C, member 2	16q24.1	2(0/1/1)

SNPs in LD with rs9929758 (count: 3) View in gBrowse (chr16:84427152..84432686 )

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