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

SNP Report

Basic Info
Name rs1569061 dbSNP Ensembl
Location chr7:73114481(Fwd)
Variant Alleles C/T
Ancestral Allele C
Functional Annotation 3_prime_UTR_variant; downstream_gene_variant; intron_variant; nc_transcript_variant; NMD_transcript_variant; non_coding_exon_variant.
Consequence to Transcript 3_prime_UTR_variant(ENST00000222812; ENST00000395156)
downstream_gene_variant(ENST00000265758; ENST00000395154; ENST00000395155; ENST00000421744; ENST00000423497; ENST00000430270; ENST00000430446; ENST00000442099; ENST00000453316; ENST00000461441; ENST00000462135; ENST00000463307; ENST00000470878; ENST00000471215; ENST00000480126; ENST00000491427; ENST00000491645; ENST00000494245; ENST00000496216; ENST00000497980)
intron_variant(ENST00000423166; ENST00000436944)
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
Brookes KJ, 2005 (b) MRM P-value=0.75, Case-control P-value=0.24, TDT P-value=0.0...... MRM P-value=0.75, Case-control P-value=0.24, TDT P-value=0.04 More... was not significant in case-control analysis, but showed nom...... was not significant in case-control analysis, but showed nominal significance in TDT analysis More... Significant

SNP related genes (count: 2)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 1)

SNPs in LD with rs1569061 (count: 0) View in gBrowse (chr7:73114481..73114481 )