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

SNP Report

Basic Info
Name rs2032893 dbSNP Ensembl
Location chr5:36698622(Fwd)
Variant Alleles C/T
Ancestral Allele T
Functional Annotation downstream_gene_variant; intron_variant; nc_transcript_variant.
Consequence to Transcript downstream_gene_variant(ENST00000508745; ENST00000512329)
intron_variant(ENST00000510740)
nc_transcript_variant(ENST00000510740)
No. of Studies 2 (significant: 0; non-significant: 2; trend: 0)
Source Literature-origin

SNP related studies (count: 2)
Reference Allele Change Risk Allele Statistical Values Author Comments Result of Statistical Analysis
Turic D, 2005(a) A/G allelic TRANSMIT P-value=0.05, X2=3.71 allelic TRANSMIT P-value=0.05, X2=3.71 produced modest evidence for association, with an excess of ...... produced modest evidence for association, with an excess of transmissions of allele G More... Non-significant
Laurin N, 2008(a) C/T P-value=0.746 in the catergorical analysis, P-value>0.05 in ...... P-value=0.746 in the catergorical analysis, P-value>0.05 in the quantitative analysis More... no significant evidence of association no significant evidence of association Non-significant

SNP related genes (count: 0)

SNPs in LD with rs2032893 (count: 0) View in gBrowse (chr5:36698622..36698622 )