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

SNP Report

Basic Info
Name rs36024 dbSNP Ensembl
Location chr16:55706391(Fwd)
Variant Alleles A/G
Ancestral Allele G
Functional Annotation downstream_gene_variant; intron_variant.
Consequence to Transcript downstream_gene_variant(ENST00000568655)
intron_variant(ENST00000219833; ENST00000379906; ENST00000414754; ENST00000561820; ENST00000566163; ENST00000567238; ENST00000568529; ENST00000568943)
No. of Studies 3 (significant: 0; non-significant: 3; trend: 0)
Source Literature-origin

SNP related studies (count: 3)
Reference Allele Change Risk Allele Statistical Values Author Comments Result of Statistical Analysis
Kim JW, 2008 X2=0.197, P-value=0.657, OR=1.04 X2=0.197, P-value=0.657, OR=1.04 not associated with ADHD not associated with ADHD Non-significant
Hawi, Z., 2012 G:A P-value=1, X2=0, OR=1, 95% CI=0.77-1.29 P-value=1, X2=0, OR=1, 95% CI=0.77-1.29 The marker did not show significant association with ADHD. The marker did not show significant association with ADHD. Non-significant
Sengupta, S. M., 2012 C/T P-value=0.18, Z statistic (allele 1)=1.33 P-value=0.18, Z statistic (allele 1)=1.33 No significant association was found in this study. No significant association was found in this study. Non-significant

SNP related genes (count: 1)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 0)


SNPs in LD with rs36024 (count: 3) View in gBrowse (chr16:55696756..55706391 )
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)