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

SNP Report

Basic Info
Name rs2284411 dbSNP Ensembl
Location chr12:13866172(Fwd)
Variant Alleles C/T
Ancestral Allele T
Functional Annotation intron_variant.
Consequence to Transcript intron_variant(ENST00000609686)
No. of Studies 2 (significant: 1; non-significant: 1; trend: 0)
Source Literature-origin

SNP related studies (count: 2)
Reference Allele Change Risk Allele Statistical Values Author Comments Result of Statistical Analysis
Dorval KM, 2007 T/C C Allelic TDT P-value=0.005 Allelic TDT P-value=0.005 Significant TDT results Significant TDT results Significant
Park, S.,2013 C/T allelic P-value=0.281 (Cohen`s w=0.04;X2=1.16);ge...... allelic P-value=0.281 (Cohen`s w=0.04;X2=1.16);genotypic P-value=0.469 (Cohen`s w=0.06;X2=1.52);TDT P-value=0.331,Cohen`s w=0.06, X2=0.94. More... This SNP was not significant associated with ADHD This SNP was not significant associated with ADHD Non-significant

SNP related genes (count: 1)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 0)


SNPs in LD with rs2284411 (count: 10) View in gBrowse (chr12:13857007..13872044 )
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: 10)