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

SNP Report

Basic Info
Name rs11659017 dbSNP Ensembl
Location chr17:79018379(Fwd)
Variant Alleles C/T
Ancestral Allele C
Functional Annotation intron_variant; nc_transcript_variant; NMD_transcript_variant.
Consequence to Transcript intron_variant(ENST00000321280; ENST00000321300; ENST00000392411; ENST00000428708; ENST00000435091; ENST00000570913; ENST00000571530; ENST00000572329; ENST00000573894; ENST00000575245; ENST00000575712; ENST00000575750; ENST00000575989; ENST00000576470)
nc_transcript_variant(ENST00000570913; ENST00000573894; ENST00000576470)
NMD_transcript_variant(ENST00000572329; ENST00000575750)
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
Ribases M, 2009(a) Case-control test: P-value=0.82 for genotype analysis, P-val...... Case-control test: P-value=0.82 for genotype analysis, P-value=0.52 for allele analysis in Spanish adult ADHD group; P-value=0.83 for genotype analysis, P-value=0.85 for allele analysis in Spanish childhood ADHD group; P-value=0.58 for genotype analysis, P-value=0.31 for allele analysis in German adult ADHD group; P-value=0.59 for genotype analysis, P-value=1.00 for allele analysis in Norwegian adult ADHD group. More... No association was found. No association was found. Non-significant

SNP related genes (count: 1)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 0)

SNPs in LD with rs11659017 (count: 1) View in gBrowse (chr17:79018379..79026485 )
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)