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

SNP Report

Basic Info
Name rs2020942 dbSNP Ensembl
Location chr17:28546914(Fwd)
Variant Alleles C/T
Ancestral Allele C
Functional Annotation intron_variant.
Consequence to Transcript intron_variant(ENST00000261707; ENST00000394821; ENST00000401766)
No. of Studies 2 (significant: 0; non-significant: 2; trend: 0)
Source Literature-origin

SNP related studies (count: 2)
Reference Allele Change Risk Allele Statistical Values Author Comments Result of Statistical Analysis
Brookes K, 2006 A/G UNPHASED TDT P-value=0.195; WHAP TDT P-value=0.309 UNPHASED TDT P-value=0.195; WHAP TDT P-value=0.309 no significant association was observed no significant association was observed Non-significant
Landaas ET, 2010 A/G P-value=0.43, OR=0.93 in the Norwegian samples; P-value=0.61...... P-value=0.43, OR=0.93 in the Norwegian samples; P-value=0.61, OR=0.94 in the Norwegian samples; P-value=0.63, OR=0.94 in the Norwegian males More... no significant association no significant association Non-significant

SNP related genes (count: 1)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 0)


SNPs in LD with rs2020942 (count: 0) View in gBrowse (chr17:28546914..28546914 )