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

SNP Report

Basic Info
Name rs916455 dbSNP Ensembl
Location chr11:636929(Fwd)
Variant Alleles C/T
Ancestral Allele C
Functional Annotation upstream_gene_variant.
Consequence to Transcript upstream_gene_variant(ENST00000176183; ENST00000528733)
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
Yang JW, 2008 C/T Fisher's exact test, P-value=0.838 and X2 =0.013,...... Fisher's exact test, P-value=0.838 and X2 =0.013, P-value=0.910 for genotypes and alleles More... no evidence for association no evidence for association Non-significant
Nyman ES, 2007 No available information. No available information. No evidence of association was seen. No evidence of association was seen. Non-significant

SNP related genes (count: 1)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 0)


SNPs in LD with rs916455 (count: 0) View in gBrowse (chr11:636929..636929 )