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

SNP Report

Basic Info
Name rs9930182 dbSNP Ensembl
Location chr16:55741297(Fwd)
Variant Alleles T/G
Ancestral Allele T
Functional Annotation downstream_gene_variant.
Consequence to Transcript downstream_gene_variant(ENST00000219833; ENST00000379906; ENST00000414754; ENST00000561820; ENST00000567238; ENST00000574918)
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 T:G T P-value=0.0562, X2=3.65, OR=1.36, 95% CI=0.99-1.8...... P-value=0.0562, X2=3.65, OR=1.36, 95% CI=0.99-1.86 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 rs9930182 (count: 22) View in gBrowse (chr16:55717483..55782138 )
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: 22)