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

SNP Report

Basic Info
Name rs4591778 dbSNP Ensembl
Location chr5:36608165(Fwd)
Variant Alleles C/T
Ancestral Allele C
Functional Annotation intron_variant; nc_transcript_variant; upstream_gene_variant.
Consequence to Transcript intron_variant(ENST00000265113; ENST00000416645; ENST00000504121; ENST00000505202; ENST00000506725; ENST00000512374; ENST00000513903)
nc_transcript_variant(ENST00000504121; ENST00000506725; ENST00000512374)
upstream_gene_variant(ENST00000381918; ENST00000502864; ENST00000513646; ENST00000514563)
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) C/T P-value=0.78 for pooled genotyping P-value=0.78 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 rs4591778 (count: 12) View in gBrowse (chr5:36602563..36608165 )
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: 12)