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

SNP Report

Basic Info
Name rs206936 dbSNP Ensembl
Location chr6:34302869(Fwd)
Variant Alleles A/G
Ancestral Allele G
Functional Annotation intron_variant.
Consequence to Transcript intron_variant(ENST00000605528; ENST00000607016)
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
Albayrak O., 2013 ADHD risk, P-value=3.4E-04, corrected P-value=0.01, OR=1.39;...... ADHD risk, P-value=3.4E-04, corrected P-value=0.01, OR=1.39; Association to ADHD subphenotypes in the German sample, inattention, P-value=0.02, hyperactivity/impulsivity P-value=0.28; Association to ADHD subphenotypes in ADHD meta-analysis data, inattention, P-value=0.09, hyperactivity/impulsivity P-value=0.7, inattention and hyperactivity/impulsivity, P-value=0.54 More... We detected association with an increased risk for ADHD for ...... We detected association with an increased risk for ADHD for the obesity risk allele G at SNP rs206936. The BMI SNP risk alleles were associated with the quantitative trait inattention with uncorrected P-values below 0.05. More... Significant

SNP related genes (count: 2)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 1)


SNPs in LD with rs206936 (count: 32) View in gBrowse (chr6:34255476..34405715 )
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: 32)