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

SNP Report

Basic Info
Name rs10503800 dbSNP Ensembl
Location chr8:26695617(Fwd)
Variant Alleles C/A
Ancestral Allele C
Functional Annotation intron_variant; nc_transcript_variant; NMD_transcript_variant; upstream_gene_variant.
Consequence to Transcript intron_variant(ENST00000276393; ENST00000354550; ENST00000380572; ENST00000380573; ENST00000380581; ENST00000380582; ENST00000380586; ENST00000380587; ENST00000518621; ENST00000519096; ENST00000519229; ENST00000521711)
nc_transcript_variant(ENST00000518621)
NMD_transcript_variant(ENST00000519096; ENST00000521711)
upstream_gene_variant(ENST00000519826)
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
Hawi, Z., 2012 C:A C P-value=0.0219*, X2=5.26, OR=1.37, 95% CI=1.04-1....... P-value=0.0219*, X2=5.26, OR=1.37, 95% CI=1.04-1.78 More... Nominal associations between ADHD and the marker was observe...... Nominal associations between ADHD and the marker was observed. However, the association did not remain significant after adjusting the p values using 10,000 permutations. More... Significant

SNP related genes (count: 3)

Literature-origin genes (count: 2)

Genes from other sources Help (count: 1)


SNPs in LD with rs10503800 (count: 2) View in gBrowse (chr8:26695617..26712981 )
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: 2)