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

SNP Report

Basic Info
Name rs5016282 dbSNP Ensembl
Location Chr11:88741660(Fwd)
Variant Alleles A/G
Ancestral Allele A
Functional Annotation intron_variant.
Consequence to Transcript intron_variant(ENST00000305432; ENST00000393294; ENST00000393297; ENST00000305447; ENST00000449371; ENST00000418177; ENST00000455756)
No. of Studies 1 (significant: 0; non-significant: 0; trend: 1)
Source Literature-origin

SNP related studies (count: 1)
Reference Allele Change Risk Allele Statistical Values Author Comments Result of Statistical Analysis
Hinney, A., 2011 A GWAS P-value=1.78E-06, OR=1.85, Replication FBAT P-value=0.3...... GWAS P-value=1.78E-06, OR=1.85, Replication FBAT P-value=0.3428, Combination P-value=2.55E-06 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... Trend

SNP related genes (count: 1)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 0)


SNPs in LD with rs5016282 (count: 0) View in gBrowse (chr11:88741660..88741660 )