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

SNP Report

Basic Info
Name rs2129575 dbSNP Ensembl
Location chr12:72340073(Fwd)
Variant Alleles G/T
Ancestral Allele G
Functional Annotation intron_variant; nc_transcript_variant.
Consequence to Transcript intron_variant(ENST00000333850; ENST00000546576)
nc_transcript_variant(ENST00000546576)
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
Sheehan K, 2005 G/T allelic TDT P-value=0.49, X2=0.62, OR=1.16; TDT P...... allelic TDT P-value=0.49, X2=0.62, OR=1.16; TDT P-value=0.8, X2=0.19, OR=1.1 of paternal origin; TDT P-value=0.53, X2=0.61, OR=1.3 of maternal origin More... did not attain significance at P<0.05 did not attain significance at P<0.05 Non-significant

SNP related genes (count: 1)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 0)


SNPs in LD with rs2129575 (count: 6) View in gBrowse (chr12:72338628..72394299 )
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: 6)