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

SNP Report

Basic Info
Name rs13270024 dbSNP Ensembl
Location chr8:142201477(Fwd)
Variant Alleles T/C
Ancestral Allele T
Functional Annotation downstream_gene_variant; intron_variant; nc_transcript_variant; non_coding_exon_variant; upstream_gene_variant.
Consequence to Transcript downstream_gene_variant(ENST00000520571)
intron_variant(ENST00000262585; ENST00000424248; ENST00000517813; ENST00000518668; ENST00000519811; ENST00000523308)
nc_transcript_variant(ENST00000517813; ENST00000521835; ENST00000523530)
non_coding_exon_variant(ENST00000521835; ENST00000523530)
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
Hinney, A., 2011 C GWAS P-value=5.75E-05, OR=1.46 GWAS P-value=5.75E-05, OR=1.46 This GWAS in a small group of clinically ascertained young G...... This GWAS in a small group of clinically ascertained young German patients with ADHD and population-based controls did not reveal genome-wide significant findings. Replication attempts in further German and international samples did also not lead to a P-value(s) below 5E-08. More... Non-significant

SNP related genes (count: 1)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 0)

SNPs in LD with rs13270024 (count: 9) View in gBrowse (chr8:142198718..142233819 )
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: 9)