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

SNP Report

Basic Info
Name rs3817334 dbSNP Ensembl
Location chr11:47650993(Fwd)
Variant Alleles C/T
Ancestral Allele C
Functional Annotation downstream_gene_variant; intron_variant; nc_transcript_variant; upstream_gene_variant.
Consequence to Transcript downstream_gene_variant(ENST00000533571)
intron_variant(ENST00000302503; ENST00000525649; ENST00000530428; ENST00000539759; ENST00000542981)
nc_transcript_variant(ENST00000525649; ENST00000539759)
upstream_gene_variant(ENST00000534074)
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=0.09, corrected P-value=1, OR=1.14; Assoc...... ADHD risk, P-value=0.09, corrected P-value=1, OR=1.14; Association to ADHD subphenotypes in the German sample, inattention, P-value=0.35, hyperactivity/impulsivity P-value=0.19, Association to ADHD subphenotypes in ADHD meta-analysis data, inattention, P-value=0.47, hyperactivity/impulsivity P-value=0.64, inattention and hyperactivity/impulsivity, P-value=0.8 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 rs3817334 (count: 25) View in gBrowse (chr11:47454972..47807774 )
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: 25)