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

SNP Report

Basic Info
Name rs11179027 dbSNP Ensembl
Location chr12:72377312(Fwd)
Variant Alleles G/C
Ancestral Allele G
Functional Annotation intron_variant.
Consequence to Transcript intron_variant(ENST00000333850)
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
Park, T. W.,2013 G/C allelic chi-square tests P-value=0.084 (OR=1.35; 95%CI=0.96-...... allelic chi-square tests P-value=0.084 (OR=1.35; 95%CI=0.96-1.88; X2=1.73); genotypic chi-square tests P-value=0.020 (OR=2.12; 95%CI=1.13-3.97; X2=2.33). More... There was a significant difference in the frequency between ...... There was a significant difference in the frequency between the cases and controls. More... Significant

SNP related genes (count: 1)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 0)

SNPs in LD with rs11179027 (count: 38) View in gBrowse (chr12:72342284..72406833 )
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: 38)