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

SNP Report

Basic Info
Name rs4939921 dbSNP Ensembl
Location chr18:47462328(Fwd)
Variant Alleles T/C
Ancestral Allele T
Functional Annotation intron_variant.
Consequence to Transcript intron_variant(ENST00000285039)
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
Landaas ET, 2011 C P-value=0.22, OR=0.85 for frequencies of the BD risk alleles...... P-value=0.22, OR=0.85 for frequencies of the BD risk alleles and genotypes in ADHD More... did not show any association with ADHD did not show any association 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 rs4939921 (count: 4) View in gBrowse (chr18:47377751..47479491 )
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: 4)