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

SNP Report

Basic Info
Name rs787558 dbSNP Ensembl
Location chr18:11865878(Fwd)
Variant Alleles C/T
Ancestral Allele C
Functional Annotation intron_variant.
Consequence to Transcript intron_variant(ENST00000269162; ENST00000334049; ENST00000423027; ENST00000535121; ENST00000585642; ENST00000590228; ENST00000602628)
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
Laurin N, 2008(b) T/C TDT P-value=0.363, X2=0.828 TDT P-value=0.363, X2=0.828 no significant evidence of association no significant evidence of association Non-significant

SNP related genes (count: 1)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 0)


SNPs in LD with rs787558 (count: 0) View in gBrowse (chr18:11865878..11865878 )