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

SNP Report

Basic Info
Name rs6108461 dbSNP Ensembl
Location chr20:10267270(Fwd)
Variant Alleles A/G
Ancestral Allele G
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 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
Hawi, Z.,2013 A allelic:T=186 ,NT=136,X2=7.764 ,P-value=0.0053 ...... A allelic:T=186 ,NT=136,X2=7.764 ,P-value=0.0053 ,EP-value=0.06,OR=1.37 More... TDT analyses of this SNP showed significant nominal associat...... TDT analyses of this SNP showed significant nominal association with ADHD, but not significant after permutation More... Significant

SNP related genes (count: 2)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 1)

SNPs in LD with rs6108461 (count: 2) View in gBrowse (chr20:10253082..10267270 )
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: 2)