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

SNP Report

Basic Info
Name rs3785152 dbSNP Ensembl
Location chr16:55716550(Fwd)
Variant Alleles T/C
Ancestral Allele C
Functional Annotation intron_variant.
Consequence to Transcript intron_variant(ENST00000219833; ENST00000379906; ENST00000414754; ENST00000561820; ENST00000566163; ENST00000567238; ENST00000568529; ENST00000568943)
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
Kim JW, 2008 X2=3.789, P-value=0.051, OR=1.38 X2=3.789, P-value=0.051, OR=1.38 not associated with ADHD not associated with ADHD Non-significant
Sengupta, S. M., 2012 C/T P-value=0.14, Z statistic (allele 1)=1.46 P-value=0.14, Z statistic (allele 1)=1.46 No significant association was found in this study. No significant association was found in this study. Non-significant

SNP related genes (count: 1)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 0)

SNPs in LD with rs3785152 (count: 0) View in gBrowse (chr16:55716550..55716550 )