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

SNP Report

Basic Info
Name rs6077690 dbSNP Ensembl
Location chr20:10197461(Fwd)
Variant Alleles A/T
Ancestral Allele A
Functional Annotation intron_variant; nc_transcript_variant; upstream_gene_variant.
Consequence to Transcript intron_variant(ENST00000421143; ENST00000426491; ENST00000451151; ENST00000453544; ENST00000603542; ENST00000605592)
nc_transcript_variant(ENST00000421143; ENST00000426491; ENST00000451151; ENST00000453544; ENST00000603542; ENST00000605592)
upstream_gene_variant(ENST00000254976; ENST00000304886; ENST00000430336)
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
Renner TJ, 2008 FAMHAP P-value=0.86 FAMHAP P-value=0.86 no significant preferential transmissions to affected childr...... no significant preferential transmissions to affected children with ADHD were detected More... Non-significant
Kim JW, 2007 T/A A Combined TDT P-value=0.03 (OR=0.80); Single marker analysis ...... Combined TDT P-value=0.03 (OR=0.80); Single marker analysis FBAT P-value=0.375; Exploratory analyses FBAT P-value=0.301 for co-morbid CD, P-value=0.489 for co-morbid MDD, P-value=0.728 for co-morbid BD More... Combined analysis showed evidence of significant association...... Combined analysis showed evidence of significant association with ADHD More... Significant

SNP related genes (count: 2)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 1)


SNPs in LD with rs6077690 (count: 1) View in gBrowse (chr20:10195433..10197461 )
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: 1)