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

SNP Report

Basic Info
Name rs9804190 dbSNP Ensembl
Location chr10:61839831(Fwd)
Variant Alleles C/T
Ancestral Allele T
Functional Annotation downstream_gene_variant; intron_variant; upstream_gene_variant.
Consequence to Transcript downstream_gene_variant(ENST00000508449)
intron_variant(ENST00000280772; ENST00000355288; ENST00000373820; ENST00000373827; ENST00000503366; ENST00000511043)
upstream_gene_variant(ENST00000365320)
No. of Studies 1 (significant: 0; non-significant: 1; trend: 0)
Source Literature-origin

SNP related studies (count: 1)
Reference Allele Change Risk Allele Statistical Values Author Comments Result of Statistical Analysis
Landaas ET, 2011 C P-value=0.23, OR=0.89 for frequencies of the BD risk alleles...... P-value=0.23, OR=0.89 for frequencies of the BD risk alleles and genotypes in ADHD More... did not show any association with ADHD did not show any association with ADHD Non-significant

SNP related genes (count: 1)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 0)


SNPs in LD with rs9804190 (count: 0) View in gBrowse (chr10:61839831..61839831 )