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

SNP Report

Basic Info
Name rs1017753 dbSNP Ensembl
Location chr9:93377901(Fwd)
Variant Alleles C/T
Ancestral Allele T
Functional Annotation intron_variant.
Consequence to Transcript intron_variant(ENST00000375765)
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
Reif, A., 2011 C/T P-value=0.2741, OR (allele)=1.11 (C), 95% CI=0.92-1.33 in Ge...... P-value=0.2741, OR (allele)=1.11 (C), 95% CI=0.92-1.33 in German discovery sample; P-value=0.4749, OR (allele)=1.04 (C), 95% CI=0.93-1.17 in IMpACT replication sample; P-value=0.2353, OR (allele)=1.06 (C), 95% CI=0.96-1.17 in pooled data; PDT P-value=0.6911 for allele T in the family-based analysis More... This SNP did not reach p<0.05 in the association test with a...... This SNP did not reach 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... Non-significant

SNP related genes (count: 1)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 0)

SNPs in LD with rs1017753 (count: 1) View in gBrowse (chr9:93377901..93380772 )
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)