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

SNP Report

Basic Info
Name rs4869686 dbSNP Ensembl
Location chr5:36679018(Fwd)
Variant Alleles A/T
Ancestral Allele T
Functional Annotation downstream_gene_variant; intron_variant; nc_transcript_variant; upstream_gene_variant.
Consequence to Transcript downstream_gene_variant(ENST00000505376)
intron_variant(ENST00000265113; ENST00000381918; ENST00000510740)
nc_transcript_variant(ENST00000510740)
upstream_gene_variant(ENST00000506178)
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
Turic D, 2005(a) A/T P-value=0.56 for pooled genotyping P-value=0.56 for pooled genotyping not significantly associated with ADHD not significantly associated with ADHD Non-significant

SNP related genes (count: 1)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 0)


SNPs in LD with rs4869686 (count: 8) View in gBrowse (chr5:36662889..36807189 )
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: 8)