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

SNP Report

Basic Info
Name rs6892282 dbSNP Ensembl
Location chr5:159360485(Fwd)
Variant Alleles G/T
Ancestral Allele T
Functional Annotation intron_variant.
Consequence to Transcript intron_variant(ENST00000306675)
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:T G P-value=0.1151, X2=2.48, OR=1.23, 95% CI=0.95-1.5...... P-value=0.1151, X2=2.48, OR=1.23, 95% CI=0.95-1.59 More... 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 rs6892282 (count: 2) View in gBrowse (chr5:159339533..159360485 )
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: 2)