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

SNP Report

Basic Info
Name rs498793 dbSNP Ensembl
Location chr11:61624705(Fwd)
Variant Alleles T/C
Ancestral Allele T
Functional Annotation intron_variant; nc_transcript_variant; upstream_gene_variant.
Consequence to Transcript intron_variant(ENST00000257261; ENST00000278840; ENST00000355484; ENST00000521571; ENST00000521849; ENST00000522056; ENST00000523235)
nc_transcript_variant(ENST00000523235)
upstream_gene_variant(ENST00000522359)
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
Brookes KJ, 2006(a) C/T allelic P-value=0.0037, OR=1.6; TDT P-value=0.013, OR=1.69 (...... allelic P-value=0.0037, OR=1.6; TDT P-value=0.013, OR=1.69 (C allele), OR=0.53 (T allele); HHRR P-value=0.018, OR=1.2 (C allele), OR=0.75 (T allele) More... significant association with ADHD was detected in both case-...... significant association with ADHD was detected in both case-control and within-family analyses More... Significant
Brookes K, 2006 A/G UNPHASED TDT P-value=0.45; WHAP TDT P-value=0.116 UNPHASED TDT P-value=0.45; WHAP TDT P-value=0.116 no significant association was observed no significant association was observed Non-significant

SNP related genes (count: 1)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 0)


SNPs in LD with rs498793 (count: 0) View in gBrowse (chr11:61624705..61624705 )