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

SNP Report

Basic Info
Name rs42460 dbSNP Ensembl
Location chr16:55737656(Fwd)
Variant Alleles G/A
Ancestral Allele A
Functional Annotation 3_prime_UTR_variant; downstream_gene_variant; intron_variant.
Consequence to Transcript 3_prime_UTR_variant(ENST00000379906; ENST00000414754; ENST00000567238)
downstream_gene_variant(ENST00000566163; ENST00000568943)
intron_variant(ENST00000219833; ENST00000561820; ENST00000574918)
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
Kim JW, 2008 X2=0.883, P-value=0.347, OR=1.17 X2=0.883, P-value=0.347, OR=1.17 not associated with ADHD not 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 rs42460 (count: 10) View in gBrowse (chr16:55735538..55783706 )
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: 10)