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

SNP Report

Basic Info
Name rs4771122 dbSNP Ensembl
Location chr13:28020180(Fwd)
Variant Alleles G/A
Ancestral Allele G
Functional Annotation intron_variant; nc_transcript_variant; upstream_gene_variant.
Consequence to Transcript intron_variant(ENST00000381116; ENST00000381120; ENST00000405591; ENST00000431572; ENST00000460973; ENST00000461838; ENST00000464753; ENST00000471771; ENST00000484342; ENST00000485650; ENST00000485959; ENST00000493719)
nc_transcript_variant(ENST00000460973; ENST00000461838; ENST00000464753; ENST00000471771; ENST00000484342; ENST00000485650; ENST00000485959; ENST00000493719)
upstream_gene_variant(ENST00000483903)
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=0.78; Association to ADHD subphenotypes i...... ADHD risk, P-value=0.78; Association to ADHD subphenotypes in the German sample, inattention, P-value=0.04, hyperactivity/impulsivity P-value=0.97; Association to ADHD subphenotypes in ADHD meta-analysis data, inattention, P-value=0.31, hyperactivity/impulsivity P-value=0.28, inattention and hyperactivity/impulsivity, P-value=0.19 More... The BMI SNP risk alleles were associated with the quantitati...... The BMI SNP risk alleles were associated with the quantitative trait inattention with uncorrected P-values below 0.05. More... Significant

SNP related genes (count: 1)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 0)


SNPs in LD with rs4771122 (count: 10) View in gBrowse (chr13:28000282..28047269 )
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: 10)