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

SNP Report

Basic Info
Name rs333229 dbSNP Ensembl
Location chr2:108631384(Fwd)
Variant Alleles G/T
Ancestral Allele G
Functional Annotation downstream_gene_variant.
Consequence to Transcript downstream_gene_variant(ENST00000264047; ENST00000409059; ENST00000540517)
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
English BA, 2009 A/G Case-control allelic test: P-value=0.008 for Caucasian group...... Case-control allelic test: P-value=0.008 for Caucasian group, P-value=0.004 for Caucasian-male group; family-based allelic test: TDT minimum P-value=0.347 under a dominant model More... a significant decrease of the 3'SNP minor allele in Caucasia...... a significant decrease of the 3'SNP minor allele in Caucasian male subjects More... Significant

SNP related genes (count: 1)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 0)


SNPs in LD with rs333229 (count: 3) View in gBrowse (chr2:108631051..108635697 )
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: 3)