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

SNP Report

Basic Info
Name rs34246405 dbSNP Ensembl
Location chr4:62812738(Fwd)
Variant Alleles T/C
Ancestral Allele T
Functional Annotation nc_transcript_variant; non_coding_exon_variant; synonymous_variant.
Consequence to Transcript nc_transcript_variant(ENST00000508078)
non_coding_exon_variant(ENST00000508078)
synonymous_variant(ENST00000502815; ENST00000504896; ENST00000506700; ENST00000506720; ENST00000506746; ENST00000507164; ENST00000507625; ENST00000508693; ENST00000508946; ENST00000509896; ENST00000511324; ENST00000512091; ENST00000514157; ENST00000514591; ENST00000514996; ENST00000545650)
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.2322T>C ObsHET/PredHET=2/178 ObsHET/PredHET=2/178 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 rs34246405 (count: 0) View in gBrowse (chr4:62812738..62812738 )