ADHDgene Database
  • Published Variant
  • Published Gene: 359
  • Published Region: 128
  • Pathway by PBA: 8
  • Study: 361

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)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 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.

Literature-origin SNPs (count: 0)

LD-proxies (count: 1)