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

SNP Report

Basic Info
Name rs8079781 dbSNP Ensembl
Location chr17:79050148(Fwd)
Variant Alleles C/T
Ancestral Allele C
Functional Annotation intron_variant; nc_transcript_variant; NMD_transcript_variant; non_coding_exon_variant.
Consequence to Transcript intron_variant(ENST00000321280; ENST00000321300; ENST00000392411; ENST00000428708; ENST00000435091; ENST00000571530; ENST00000572073; ENST00000572329; ENST00000572918; ENST00000573017; ENST00000573659; ENST00000573677; ENST00000573894; ENST00000574804; ENST00000575245; ENST00000575712; ENST00000575750; ENST00000575958; ENST00000575989; ENST00000576364; ENST00000576470)
nc_transcript_variant(ENST00000570913; ENST00000573017; ENST00000573894; ENST00000576364; ENST00000576470)
NMD_transcript_variant(ENST00000572329; ENST00000574804; ENST00000575750)
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
Ribases M, 2009(a) Case-control test: P-value=0.01 for genotype analysis, P-val...... Case-control test: P-value=0.01 for genotype analysis, P-value=0.01 for allele analysis in Spanish adult ADHD group; P-value=0.97 for genotype analysis, P-value=0.82 for allele analysis in Spanish childhood ADHD group; P-value=0.19 for genotype analysis, P-value=0.24 for allele analysis in German adult ADHD group; P-value=0.74 for genotype analysis, P-value=0.61 for allele analysis in Norwegian adult ADHD group. More... significant associations with adult ADHD were found both in ...... significant associations with adult ADHD were found both in Spanish and German population More... Significant

SNP related genes (count: 1)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 0)

SNPs in LD with rs8079781 (count: 7) View in gBrowse (chr17:79050148..79095144 )
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: 7)