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

SNP Report

Basic Info
Name rs10968576 dbSNP Ensembl
Location chr9:28414339(Fwd)
Variant Alleles A/G
Ancestral Allele A
Functional Annotation intron_variant.
Consequence to Transcript intron_variant(ENST00000379992)
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=0.63, corrected P-value=1, OR=1.04; Assoc...... ADHD risk, P-value=0.63, corrected P-value=1, OR=1.04; Association to ADHD subphenotypes in the German sample, inattention, P-value=1, hyperactivity/impulsivity P-value=1; Association to ADHD subphenotypes in ADHD meta-analysis data, inattention, P-value=0.74, hyperactivity/impulsivity P-value=0.98, inattention and hyperactivity/impulsivity, P-value=0.66 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 rs10968576 (count: 21) View in gBrowse (chr9:28410683..28492396 )
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: 21)