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

SNP Report

Basic Info
Name rs4860 dbSNP Ensembl
Location chr12:63359783(Fwd); chr3:40503754(Fwd)
Variant Alleles C/T
Ancestral Allele T
Functional Annotation downstream_gene_variant; 3_prime_UTR_variant; nc_transcript_variant; non_coding_exon_variant; upstream_gene_variant.
Consequence to Transcript downstream_gene_variant(ENST00000266610; ENST00000484568)
3_prime_UTR_variant(ENST00000338970; ENST00000396203; ENST00000416518; ENST00000435633; ENST00000461368; ENST00000465280; ENST00000465325; ENST00000481798)
nc_transcript_variant(ENST00000479563)
non_coding_exon_variant(ENST00000479563)
upstream_gene_variant(ENST00000607057)
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
Wang G. X., 2012 A/G A Chi-square test: genotypic p>0.05; allelic p>0.05 Chi-square test: genotypic p>0.05; allelic p>0.05 The genotype distribution and allele frequencies of this SNP...... The genotype distribution and allele frequencies of this SNP showed no significant difference between ADHD children and healthy controls. More... Non-significant

SNP related genes (count: 3)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 2)


SNPs in LD with rs4860 (count: 0) View in gBrowse (chr3:40503754..40503754 )