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

SNP Report

Basic Info
Name rs7036351 dbSNP Ensembl
Location chr9:34592699(Fwd)
Variant Alleles C/T
Ancestral Allele C
Functional Annotation upstream_gene_variant.
Consequence to Transcript upstream_gene_variant(ENST00000351266; ENST00000378980; ENST00000417345)
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=2.5e-04; genotypic P-value=0.0037, OR=1.69...... genotypic P-value=2.5e-04; genotypic P-value=0.0037, OR=1.69 (1.18-2.44) in dominant model; genotypic P-value=0.058 in recessive model; allelic P-value=0.062 in Adults; genotypic P-value=0.073; genotypic P-value=0.022, OR=1.41 (1.05-1.92) in dominant model; genotypic P-value=0.057 in recessive model; allelic P-value=0.03, OR=1.33 (1.02-1.75) in Children More... provided evidence of association with adulthood and childhoo...... provided evidence of association with adulthood and childhood ADHD More... Significant

SNP related genes (count: 1)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 0)

SNPs in LD with rs7036351 (count: 10) View in gBrowse (chr9:34592699..34690811 )
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: 10)