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

SNP Report

Basic Info
Name rs16906711 dbSNP Ensembl
Location chr9:93373278(Fwd)
Variant Alleles C/G
Ancestral Allele C
Functional Annotation 3_prime_UTR_variant.
Consequence to Transcript 3_prime_UTR_variant(ENST00000375765)
No. of Studies 1 (significant: 1; non-significant: 0; trend: 0)
Source Literature-origin

SNP related studies (count: 1)
Reference Allele Change Risk Allele Statistical Values Author Comments Result of Statistical Analysis
Reif, A., 2011 C/G P-value=0.0453, OR (allele)=1.97 (G), 95% CI=1.01-3.81 in Ge...... P-value=0.0453, OR (allele)=1.97 (G), 95% CI=1.01-3.81 in German discovery sample; P-value=0.7288, OR (allele)=1.07 (C), 95% CI=0.74-1.55 in IMpACT replication sample; P-value=0.4271, OR (allele)=1.14 (G), 95% CI=0.83-1.55 in pooled data; PDT P-value=0.3711 for allele C in the family-based analysis More... 4 out of 12 investigated SNPs had p<0.05 in the association ...... 4 out of 12 investigated SNPs had p<0.05 in the association test with aADHD. Replication in 1035 aADHD patients and 1381 controls from IMpACT did not show any significant SNP association. More... Significant

SNP related genes (count: 1)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 0)


SNPs in LD with rs16906711 (count: 3) View in gBrowse (chr9:93348404..93382438 )
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: 3)