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

SNP Report

Basic Info
Name rs6039820 dbSNP Ensembl
Location chr20:10282027(Fwd)
Variant Alleles C/T
Ancestral Allele T
Functional Annotation intron_variant; nc_transcript_variant.
Consequence to Transcript intron_variant(ENST00000254976; ENST00000304886; ENST00000421143; ENST00000453544; ENST00000495883)
nc_transcript_variant(ENST00000421143; ENST00000453544; ENST00000495883)
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
Hawi, Z.,2013 C allelic:T=152,NT=136,X2=0.889,P-value=0.3458 ,E...... C allelic:T=152,NT=136,X2=0.889,P-value=0.3458 ,EP-value=1.0,OR= 1.11 More... TDT analyses of this SNP showed no significant nominal assoc...... TDT analyses of this SNP showed no significant nominal association with ADHD More... Non-significant

SNP related genes (count: 2)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 1)

SNPs in LD with rs6039820 (count: 0) View in gBrowse (chr20:10282027..10282027 )