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

SNP Report

Basic Info
Name rs2381164 dbSNP Ensembl
Location chr9:34553968(Fwd)
Variant Alleles G/C
Ancestral Allele G
Functional Annotation downstream_gene_variant; intron_variant.
Consequence to Transcript downstream_gene_variant(ENST00000417345)
intron_variant(ENST00000351266; ENST00000378980)
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=0.03; genotypic P-value=0.083 in dominant ...... genotypic P-value=0.03; genotypic P-value=0.083 in dominant model; genotypic P-value=0.015, OR=1.69 (1.11-2.56) in recessive model; allelic P-value=0.015, OR=1.28 (1.05-1.59) in Children More... provided evidence of association with childhood ADHD provided evidence of association with childhood ADHD Significant

SNP related genes (count: 1)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 0)


SNPs in LD with rs2381164 (count: 7) View in gBrowse (chr9:34550295..34572767 )
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: 7)