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

SNP Report

Basic Info
Name rs4469933 dbSNP Ensembl
Location chr12:72414717(Fwd)
Variant Alleles C/T
Ancestral Allele C
Functional Annotation intron_variant.
Consequence to Transcript intron_variant(ENST00000333850)
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
Park, T. W.,2013 T/C allelic chi-square tests P-value=0.786 (OR=1.05; 95%CI=0.75-...... allelic chi-square tests P-value=0.786 (OR=1.05; 95%CI=0.75-1.46; X2=0.27); genotypic chi-square tests P-value=0.365 (OR=1.30; 95%CI=0.74-2.28; X2=0.91). More... No significant difference was reported in this study. No significant difference was reported in this study. Non-significant

SNP related genes (count: 1)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 0)

SNPs in LD with rs4469933 (count: 15) View in gBrowse (chr12:72410021..72416235 )
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: 15)