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

SNP Report

Basic Info
Name rs2268115 dbSNP Ensembl
Location chr12:13869725(Fwd)
Variant Alleles G/T
Ancestral Allele C
Functional Annotation intron_variant.
Consequence to Transcript intron_variant(ENST00000609686)
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
Dorval KM, 2007 T/G T Allelic TDT P-value=0.021 Allelic TDT P-value=0.021 Significant TDT results Significant TDT results Significant

SNP related genes (count: 0)

SNPs in LD with rs2268115 (count: 7) View in gBrowse (chr12:13858822..13869725 )
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: 7)