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

SNP Report

Basic Info
Name rs9816226 dbSNP Ensembl
Location chr3:185834499(Fwd)
Variant Alleles A/T
Ancestral Allele T
Functional Annotation intron_variant; nc_transcript_variant.
Consequence to Transcript intron_variant(ENST00000447054)
nc_transcript_variant(ENST00000447054)
No. of Studies 1 (significant: 1; non-significant: 0; trend: 0)
Source Literature-origin

SNP related studies (count: 1)
Reference Allele Change Risk Allele Statistical Values Author Comments Result of Statistical Analysis
Albayrak O., 2013 ADHD risk, P-value=0.03, corrected P-value=0.96, OR=0.81; As...... ADHD risk, P-value=0.03, corrected P-value=0.96, OR=0.81; Association to ADHD subphenotypes in the German sample, inattention, P-value=0.96, hyperactivity/impulsivity P-value=0.63 More... Association with an increased risk for ADHD for the obesity ...... Association with an increased risk for ADHD for the obesity risk allele was detected before multiple correction. More... Significant

SNP related genes (count: 2)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 1)


SNPs in LD with rs9816226 (count: 0) View in gBrowse (chr3:185834499..185834499 )