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

SNP Report

Basic Info
Name rs863126 dbSNP Ensembl
Location chr5:174863348(Fwd)
Variant Alleles A/T
Ancestral Allele A
Functional Annotation downstream_gene_variant.
Consequence to Transcript downstream_gene_variant(ENST00000393752)
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., 2012 genotypic P-value=0.0066, genotype 11 vs 12+22: P-value=0.01...... genotypic P-value=0.0066, genotype 11 vs 12+22: P-value=0.016, OR (95% CI)=1.47 (1.07-2.0); genotype 11 +12 vs. 22: P-value=0.23, OR (95% CI)=-; allelic P-value=0.24, OR (95% CI)=- More... Four SNPs in DRD1 displayed nominal associations with ADHD i...... Four SNPs in DRD1 displayed nominal associations with ADHD in the childhood dataset More... Significant

SNP related genes (count: 1)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 0)


SNPs in LD with rs863126 (count: 1) View in gBrowse (chr5:174859162..174863348 )
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)