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

SNP Report

Basic Info
Name rs1938526 dbSNP Ensembl
Location chr10:62300383(Fwd)
Variant Alleles A/G
Ancestral Allele A
Functional Annotation intron_variant; nc_transcript_variant.
Consequence to Transcript intron_variant(ENST00000373827; ENST00000503366; ENST00000510382)
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
Schimmelmann, B. G.,2013 Nominal two-sided P-value=0.683 (OR=1.06;95%CI=0.79-1.41) Nominal two-sided P-value=0.683 (OR=1.06;95%CI=0.79-1.41) No evidence for association was found with ADHD for the rema...... No evidence for association was found with ADHD for the remaining eight SNPs, which were found to be genome-wide significant for BD in international GWAS More... Non-significant

SNP related genes (count: 1)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 0)

SNPs in LD with rs1938526 (count: 22) View in gBrowse (chr10:62146576..62433440 )
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: 22)