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

SNP Report

Basic Info
Name rs550942 dbSNP Ensembl
Location chr11:58394154(Fwd)
Variant Alleles C/T
Ancestral Allele T
Functional Annotation downstream_gene_variant.
Consequence to Transcript downstream_gene_variant(ENST00000361987; ENST00000389919; ENST00000422974)
No. of Studies 1 (significant: 1; non-significant: 0; trend: 0)
Source Literature-origin

SNP related studies (count: 1)
Reference Allele Change Risk Allele Statistical Values Author Comments Result of Statistical Analysis
Ribases M, 2008 genotypic P-value=0.019; genotypic P-value=0.006, OR=1.64 (1...... genotypic P-value=0.019; genotypic P-value=0.006, OR=1.64 (1.15-2.38) in dominant model; genotypic P-value=0.77 in recessive model; allelic P-value=0.013, OR=1.48 (1.08-2.04) in Adults More... provided evidence of association with adulthood ADHD provided evidence of association with adulthood ADHD Significant

SNP related genes (count: 2)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 1)


SNPs in LD with rs550942 (count: 1) View in gBrowse (chr11:58394154..58415508 )
The LD data used here is based on HapMap rel#27. LD SNP pairs were selected with a threshold r2>=0.8.

Literature-origin SNPs (count: 0)

LD-proxies (count: 1)