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

SNP Report

Basic Info
Name rs7340679 dbSNP Ensembl
Location chr3:15346700(Fwd)
Variant Alleles C/T
Ancestral Allele T
Functional Annotation intron_variant; nc_transcript_variant; NMD_transcript_variant.
Consequence to Transcript intron_variant(ENST00000253688; ENST00000383791; ENST00000408919; ENST00000412806; ENST00000426925; ENST00000450625; ENST00000459627; ENST00000465894)
nc_transcript_variant(ENST00000459627; ENST00000465894)
NMD_transcript_variant(ENST00000412806; ENST00000450625)
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
Neale BM, 2010 (a) T:C P-value=1.04E-05 P-value=1.04E-05 one of top 50 hits from the Genome-Wide Attention-Deficit/Hy...... one of top 50 hits from the Genome-Wide Attention-Deficit/Hyperactivity Disorder (ADHD) meta-analysis More... Trend

SNP related genes (count: 1)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 0)

SNPs in LD with rs7340679 (count: 0) View in gBrowse (chr3:15346700..15346700 )