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

SNP Report

Basic Info
Name rs994856 dbSNP Ensembl
Location chr13:42708451(Fwd)
Variant Alleles A/G
Ancestral Allele A
Functional Annotation intron_variant; upstream_gene_variant.
Consequence to Transcript intron_variant(ENST00000261491; ENST00000337343; ENST00000379274; ENST00000540693)
upstream_gene_variant(ENST00000536612)
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
Weber H, 2011 G/A Nominal P-value=0.012, Bonferroni P-value=0.277 Nominal P-value=0.012, Bonferroni P-value=0.277 significantly associated with ADHD but was not significant f...... significantly associated with ADHD but was not significant following Bonferroni correction More... Significant

SNP related genes (count: 1)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 0)


SNPs in LD with rs994856 (count: 10) View in gBrowse (chr13:42703394..42726974 )
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)