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

SNP Report

Basic Info
Name rs3808585 dbSNP Ensembl
Location chr8:26724326(Fwd)
Variant Alleles C/T
Ancestral Allele C
Functional Annotation intron_variant; upstream_gene_variant.
Consequence to Transcript intron_variant(ENST00000380573)
upstream_gene_variant(ENST00000276393; ENST00000354550; ENST00000358857; ENST00000380572; ENST00000380581; ENST00000380582; ENST00000380586; ENST00000380587; ENST00000519096; ENST00000519229; ENST00000521711)
No. of Studies 1 (significant: 0; non-significant: 1; trend: 0)
Source Literature-origin

SNP related studies (count: 1)
Reference Allele Change Risk Allele Statistical Values Author Comments Result of Statistical Analysis
Hawi, Z., 2012 C:T C P-value=0.829, X2=0.05, OR=1.03, 95% CI=0.77-1.37 P-value=0.829, X2=0.05, OR=1.03, 95% CI=0.77-1.37 The marker did not show significant association with ADHD. The marker did not show significant association with ADHD. Non-significant

SNP related genes (count: 2)

Literature-origin genes (count: 2)

Genes from other sources Help (count: 0)


SNPs in LD with rs3808585 (count: 1) View in gBrowse (chr8:26724326..26725568 )
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)