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

SNP Report

Basic Info
Name rs1386498 dbSNP Ensembl
Location chr12:72398143(Fwd)
Variant Alleles A/G
Ancestral Allele A
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 G/A allelic chi-square tests P-value=0.520 (OR=1.12; 95%CI=0.80-...... allelic chi-square tests P-value=0.520 (OR=1.12; 95%CI=0.80-1.56; X2=0.64); genotypic chi-square tests P-value=0.084 (OR=1.65; 95%CI=0.94-2.90; X2=1.73). 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 rs1386498 (count: 26) View in gBrowse (chr12:72346800..72407477 )
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: 26)