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

SNP Report

Basic Info
Name rs2856811 dbSNP Ensembl
Location chr1:115838282(Fwd)
Variant Alleles G/T
Ancestral Allele G
Functional Annotation intron_variant; nc_transcript_variant.
Consequence to Transcript intron_variant(ENST00000369512; ENST00000425449; LRG_260t1)
nc_transcript_variant(ENST00000425449)
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
Ribases M, 2008 genotypic P-value=0.025; genotypic P-value=0.01, OR=1.46 (1....... genotypic P-value=0.025; genotypic P-value=0.01, OR=1.46 (1.09-1.94) in dominant model; genotypic P-value=0.96 in recessive model; allelic P-value=0.076 in Children More... provided evidence of association with childhood ADHD provided evidence of association with childhood ADHD Significant

SNP related genes (count: 1)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 0)


SNPs in LD with rs2856811 (count: 2) View in gBrowse (chr1:115837919..115839671 )
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: 2)