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

SNP Report

Basic Info
Name rs6133098 dbSNP Ensembl
Location chr20:4217249(Fwd)
Variant Alleles G/C
Ancestral Allele G
Functional Annotation intron_variant.
Consequence to Transcript intron_variant(ENST00000379453)
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
Hawi, Z., 2012 G:C G P-value=0.887, X2=0.02, OR=1.02, 95% CI=0.77-1.34 P-value=0.887, X2=0.02, OR=1.02, 95% CI=0.77-1.34 The marker did not show significant association with ADHD. The marker did not show significant association 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 rs6133098 (count: 0) View in gBrowse (chr20:4217249..4217249 )