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

SNP Report

Basic Info
Name rs17110747 dbSNP Ensembl
Location chr12:72425954(Fwd)
Variant Alleles G/A
Ancestral Allele G
Functional Annotation 3_prime_UTR_variant; intron_variant; nc_transcript_variant.
Consequence to Transcript 3_prime_UTR_variant(ENST00000333850)
intron_variant(ENST00000547278; ENST00000547348; ENST00000550403; ENST00000551074)
nc_transcript_variant(ENST00000547278; ENST00000547348; ENST00000550403; ENST00000551074)
No. of Studies 3 (significant: 1; non-significant: 2; trend: 0)
Source Literature-origin

SNP related studies (count: 3)
Reference Allele Change Risk Allele Statistical Values Author Comments Result of Statistical Analysis
Brookes K, 2006 A/G UNPHASED TDT P-value=0.023; WHAP TDT P-value=0.052 UNPHASED TDT P-value=0.023; WHAP TDT P-value=0.052 significant association was observed in UNPHASED analysis significant association was observed in UNPHASED analysis Significant
Park, T. W.,2013 G/A allelic chi-square tests P-value=0.916 (OR=1.02; 95%CI=0.70-...... allelic chi-square tests P-value=0.916 (OR=1.02; 95%CI=0.70-1.50; X2=0.11); genotypic chi-square tests P-value=0.647 (OR=1.27; 95%CI=0.46-3.53; X2=0.46). More... No significant difference was reported in this study. No significant difference was reported in this study. Non-significant
Johansson S, 2010 logistic regression P-value=0.39, OR=1.12 logistic regression P-value=0.39, OR=1.12 no significant association no significant association Non-significant

SNP related genes (count: 1)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 0)


SNPs in LD with rs17110747 (count: 5) View in gBrowse (chr12:72425954..72503687 )
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: 5)