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

SNP Report

Basic Info
Name rs1012053 dbSNP Ensembl
Location chr13:42653437(Fwd)
Variant Alleles C/A
Ancestral Allele A
Functional Annotation intron_variant.
Consequence to Transcript intron_variant(ENST00000261491; ENST00000337343; ENST00000379274; ENST00000540693)
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=0.396 (OR=0.92;95%CI=0.74-1.12) Nominal two-sided P-value=0.396 (OR=0.92;95%CI=0.74-1.12) 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 rs1012053 (count: 16) View in gBrowse (chr13:42642810..42701941 )
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: 16)