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

SNP Report

Basic Info
Name rs1157690 dbSNP Ensembl
Location chr8:26610152(Fwd)
Variant Alleles C/T
Ancestral Allele C
Functional Annotation downstream_gene_variant; intron_variant; NMD_transcript_variant.
Consequence to Transcript downstream_gene_variant(ENST00000380581; ENST00000380582; ENST00000519229; ENST00000521711)
intron_variant(ENST00000380586; ENST00000380587; ENST00000519096)
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
Hawi, Z., 2012 T:C C P-value=0.7406, X2=0.11, OR=1.06, 95% CI=0.68-1.3...... P-value=0.7406, X2=0.11, OR=1.06, 95% CI=0.68-1.30 More... The marker did not show significant association with ADHD. The marker did not show significant association with ADHD. Non-significant

SNP related genes (count: 2)

Literature-origin genes (count: 2)

Genes from other sources Help (count: 0)

SNPs in LD with rs1157690 (count: 1) View in gBrowse (chr8:26605110..26610152 )
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: 1)