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

SNP Report

Basic Info
Name rs5568 dbSNP Ensembl
Location chr16:55730124(Fwd)
Variant Alleles A/C
Ancestral Allele A
Functional Annotation downstream_gene_variant; intron_variant; upstream_gene_variant.
Consequence to Transcript downstream_gene_variant(ENST00000568529)
intron_variant(ENST00000219833; ENST00000379906; ENST00000414754; ENST00000561820; ENST00000566163; ENST00000567238; ENST00000568943)
upstream_gene_variant(ENST00000574918)
No. of Studies 2 (significant: 0; non-significant: 2; trend: 0)
Source Literature-origin

SNP related studies (count: 2)
Reference Allele Change Risk Allele Statistical Values Author Comments Result of Statistical Analysis
Hawi, Z., 2012 A:C C P-value=0.3708, X2=0.8, OR=1.13, 95% CI=0.86-1.48 P-value=0.3708, X2=0.8, OR=1.13, 95% CI=0.86-1.48 The marker did not show significant association with ADHD. The marker did not show significant association with ADHD. Non-significant
Kim JW, 2008 X2=0.04, P-value=0.84, OR=1.02 X2=0.04, P-value=0.84, OR=1.02 not associated with ADHD not associated with ADHD Non-significant

SNP related genes (count: 1)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 0)


SNPs in LD with rs5568 (count: 1) View in gBrowse (chr16:55730124..55731575 )
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)