ADHDgene Database

SNP Report

Basic Info

Name	rs2773822 dbSNP Ensembl
Location	chr9:135861033(Fwd)
Variant Alleles	C/T
Ancestral Allele	C
Functional Annotation	intron_variant; upstream_gene_variant.
Consequence to Transcript	intron_variant(ENST00000339463; ENST00000372124; ENST00000450530; ENST00000534944) upstream_gene_variant(ENST00000372122; ENST00000372123)
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		C	GWAS P-value=5.04E-05, OR=1.66, Replication FBAT P-value=0.7...... GWAS P-value=5.04E-05, OR=1.66, Replication FBAT P-value=0.7357, Combination P-value=1.17E-04 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)
GFI1B	growth factor independent 1B transcription repressor	9q34.13	1(0/1/0)

SNPs in LD with rs2773822 (count: 1) View in gBrowse (chr9:135861033..135861241 )

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