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

SNP Report

Basic Info
Name rs6039769 dbSNP Ensembl
Location chr20:10198954(Fwd)
Variant Alleles A/C
Ancestral Allele C
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 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
Renner TJ, 2008 FAMHAP P-value=0.54 FAMHAP P-value=0.54 no significant preferential transmissions to affected childr...... no significant preferential transmissions to affected children with ADHD were detected More... Non-significant

SNP related genes (count: 2)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 1)


SNPs in LD with rs6039769 (count: 3) View in gBrowse (chr20:10183018..10198954 )
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)