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

SNP Report

Basic Info
Name rs11847697 dbSNP Ensembl
Location chr14:30515112(Fwd)
Variant Alleles C/T
Ancestral Allele C
Functional Annotation intron_variant; nc_transcript_variant.
Consequence to Transcript intron_variant(ENST00000549360; ENST00000549503)
nc_transcript_variant(ENST00000549360)
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
Albayrak O., 2013 ADHD risk, P-value=0.1, corrected P-value=1, OR=1.36; Associ...... ADHD risk, P-value=0.1, corrected P-value=1, OR=1.36; Association to ADHD subphenotypes in the German sample, inattention, P-value=0.5,hyperactivity/impulsivity P-value=0.15 More... No significant association was reported in this study. No significant association was reported in this study. Non-significant

SNP related genes (count: 1)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 0)


SNPs in LD with rs11847697 (count: 0) View in gBrowse (chr14:30515112..30515112 )