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

SNP Report

Basic Info
Name rs363020 dbSNP Ensembl
Location chr20:10237223(Fwd)
Variant Alleles T/A
Ancestral Allele A
Functional Annotation intron_variant; nc_transcript_variant.
Consequence to Transcript intron_variant(ENST00000254976; ENST00000304886; ENST00000421143; ENST00000430336; ENST00000453544)
nc_transcript_variant(ENST00000421143; ENST00000453544)
No. of Studies 2 (significant: 1; non-significant: 1; trend: 0)
Source Literature-origin

SNP related studies (count: 2)
Reference Allele Change Risk Allele Statistical Values Author Comments Result of Statistical Analysis
Hawi, Z.,2013 T allelic:T=75,NT=66,X2=0.574,P-value=0.4485,EP-v...... T allelic:T=75,NT=66,X2=0.574,P-value=0.4485,EP-value=0.99 ,OR=1.13 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
Brookes K, 2006 A/T UNPHASED TDT P-value=0.0346; WHAP TDT P-value=0.016 UNPHASED TDT P-value=0.0346; WHAP TDT P-value=0.016 significant association was observed in both UNPHASED and WH...... significant association was observed in both UNPHASED and WHAP analyses More... Significant

SNP related genes (count: 2)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 1)


SNPs in LD with rs363020 (count: 3) View in gBrowse (chr20:10237223..10241483 )
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)