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

SNP Report

Basic Info
Name rs10994336 dbSNP Ensembl
Location chr10:62179812(Fwd)
Variant Alleles C/T
Ancestral Allele C
Functional Annotation intron_variant.
Consequence to Transcript intron_variant(ENST00000373827; ENST00000503366)
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=0.57, OR=0.91 for frequencies of the BD risk alleles...... P-value=0.57, OR=0.91 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
Schimmelmann, B. G.,2013 Nominal two-sided P-value=0.785 (OR=1.04;95%CI=0.77-1.39) Nominal two-sided P-value=0.785 (OR=1.04;95%CI=0.77-1.39) No evidence for association was found with ADHD for the rema...... No evidence for association was found with ADHD for the remaining eight SNPs, which were found to be genome-wide significant for BD in international GWAS More... Non-significant

SNP related genes (count: 1)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 0)


SNPs in LD with rs10994336 (count: 3) View in gBrowse (chr10:62179812..62279124 )
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: 3)