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

SNP Report

Basic Info
Name rs1344706 dbSNP Ensembl
Location chr2:185778428(Fwd)
Variant Alleles A/C
Ancestral Allele A
Functional Annotation intron_variant.
Consequence to Transcript intron_variant(ENST00000302277)
No. of Studies 2 (significant: 0; non-significant: 2; trend: 0)
Source Literature-origin

SNP related studies (count: 2)
Reference Allele Change Risk Allele Statistical Values Author Comments Result of Statistical Analysis
Landaas ET, 2011 T P-value=1, OR=1 for frequencies of the BD risk alleles and g...... P-value=1, OR=1 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
Xu X, 2013 A/C Uncorrected TDT P-value=0.50 Uncorrected TDT P-value=0.50 No significance was observed No significance was observed Non-significant

SNP related genes (count: 1)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 0)


SNPs in LD with rs1344706 (count: 4) View in gBrowse (chr2:185681730..185926285 )
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)