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

SNP Report

Basic Info
Name rs7854469 dbSNP Ensembl
Location chr9:93372229(Fwd)
Variant Alleles T/A
Ancestral Allele T
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 T/A P-value=0.0394, OR (allele)=1.40 (T), 95% CI=1.02-1.93 in Ge...... P-value=0.0394, OR (allele)=1.40 (T), 95% CI=1.02-1.93 in German discovery sample; P-value=0.072, OR (allele)=1.19 (A), 95% CI=0.98-1.43 in IMpACT replication sample; P-value=0.6023, OR (allele)=1.04 (A), 95% CI=0.89-1.23 in pooled data; PDT P-value=0.2059 for allele T 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 rs7854469 (count: 1) View in gBrowse (chr9:93366369..93372229 )
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: 1)