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

SNP Report

Basic Info
Name rs11795386 dbSNP Ensembl
Location chr9:87602898(Fwd)
Variant Alleles C/T
Ancestral Allele C
Functional Annotation intron_variant.
Consequence to Transcript intron_variant(ENST00000277120; ENST00000323115; ENST00000376213; ENST00000376214)
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=0.018; genotypic P-value=0.0076, OR=1.56 (...... genotypic P-value=0.018; genotypic P-value=0.0076, OR=1.56 (1.12-2.17) in dominant model; genotypic P-value=0.13 in recessive model; allelic P-value=0.0049, OR=1.12 (1.54-2.08) 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 rs11795386 (count: 5) View in gBrowse (chr9:87585624..87619071 )
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: 5)