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

SNP Report

Basic Info
Name rs4923463 dbSNP Ensembl
Location chr11:27672500(Fwd)
Variant Alleles A/G
Ancestral Allele A
Functional Annotation downstream_gene_variant; intron_variant; nc_transcript_variant.
Consequence to Transcript downstream_gene_variant(ENST00000314915; ENST00000356660; ENST00000395978; ENST00000395980; ENST00000395981; ENST00000395983; ENST00000395986; ENST00000418212; ENST00000420794; ENST00000438929; ENST00000439476; ENST00000525528; ENST00000525950; ENST00000530786; ENST00000530861; ENST00000532997; ENST00000533131; ENST00000533246; ENST00000584049)
intron_variant(ENST00000499008; ENST00000499568; ENST00000500662; ENST00000501176; ENST00000502161; ENST00000530313; ENST00000530686; ENST00000532965)
nc_transcript_variant(ENST00000499008; ENST00000499568; ENST00000500662; ENST00000501176; ENST00000502161; ENST00000530313; ENST00000530686; ENST00000532965)
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
Lanktree M, 2008 G:A X2=3.31, P-value=0.069 in the family-based sample...... X2=3.31, P-value=0.069 in the family-based sample; X2=1.96, P-value=0.16, OR=1.43 in the case-control sample; X2=5.32, P-value=0.021, OR=1.56 in the combined samples More... showed association in the combined samples showed association in the combined samples Significant

SNP related genes (count: 2)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 1)


SNPs in LD with rs4923463 (count: 0) View in gBrowse (chr11:27672500..27672500 )