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

SNP Report

Basic Info
Name rs34586911 dbSNP Ensembl
Location chr4:62453069(Fwd)
Variant Alleles G/A
Ancestral Allele G
Functional Annotation synonymous_variant; upstream_gene_variant.
Consequence to Transcript synonymous_variant(ENST00000504896; ENST00000506700; ENST00000506720; ENST00000506746; ENST00000507164; ENST00000507625; ENST00000508693; ENST00000508946; ENST00000509896; ENST00000511324; ENST00000512091; ENST00000514157; ENST00000514591; ENST00000514996; ENST00000545650; ENST00000570545; ENST00000571630; ENST00000572079; ENST00000572342; ENST00000573720; ENST00000573738; ENST00000573960; ENST00000574812; ENST00000574839; ENST00000574919; ENST00000576028; ENST00000576325; ENST00000576469; ENST00000577151)
upstream_gene_variant(ENST00000509089; ENST00000574903)
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
Domene S, 2011 c.180G>A ObsHET/PredHET=0.251/0.252 ObsHET/PredHET=0.251/0.252 neither susceptibility nor protective haplotype alleles are ...... neither susceptibility nor protective haplotype alleles are associated with obviously significant coding region changes, or canonical splice site alterations More... Trend

SNP related genes (count: 0)

SNPs in LD with rs34586911 (count: 0) View in gBrowse (chr4:62453069..62453069 )