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

SNP Report

Basic Info
Name rs17055923 dbSNP Ensembl
Location chr8:26611846(Fwd)
Variant Alleles G/A
Ancestral Allele G
Functional Annotation downstream_gene_variant; intron_variant; NMD_transcript_variant.
Consequence to Transcript downstream_gene_variant(ENST00000380581; ENST00000380582; ENST00000519229; ENST00000521711)
intron_variant(ENST00000380586; ENST00000380587; ENST00000519096)
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
Hawi, Z., 2012 G:A G P-value=0.1748, X2=1.84, OR=1.23, 95% CI=0.91-1.6...... P-value=0.1748, X2=1.84, OR=1.23, 95% CI=0.91-1.65 More... The marker did not show significant association with ADHD. The marker did not show significant association with ADHD. Non-significant

SNP related genes (count: 2)

Literature-origin genes (count: 2)

Genes from other sources Help (count: 0)

SNPs in LD with rs17055923 (count: 0) View in gBrowse (chr8:26611846..26611846 )