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

SNP Report

Basic Info
Name rs16938747 dbSNP Ensembl
Location chr8:74879087(Fwd)
Variant Alleles C/G
Ancestral Allele C
Functional Annotation intron_variant.
Consequence to Transcript intron_variant(ENST00000284811; ENST00000518127; ENST00000519082; ENST00000519487; ENST00000520210; ENST00000520242; ENST00000522337; ENST00000523815; ENST00000602840)
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) C:G P-value=2.30E-05 P-value=2.30E-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 rs16938747 (count: 0) View in gBrowse (chr8:74879087..74879087 )