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

SNP Report

Basic Info
Name rs987237 dbSNP Ensembl
Location chr6:50803050(Fwd)
Variant Alleles A/G
Ancestral Allele A
Functional Annotation intron_variant.
Consequence to Transcript intron_variant(ENST00000263046; ENST00000393655)
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=0.74, corrected P-value=1, OR=1.03; Assoc...... ADHD risk, P-value=0.74, corrected P-value=1, OR=1.03; Association to ADHD subphenotypes in the German sample, inattention, P-value=0.04, hyperactivity/impulsivity P-value=0.46 More... The BMI SNP risk alleles were associated with the quantitati...... 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: 1)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 0)


SNPs in LD with rs987237 (count: 12) View in gBrowse (chr6:50798526..50938247 )
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: 12)