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

SNP Report

Basic Info
Name rs10492555 dbSNP Ensembl
Location chr13:36709109(Fwd)
Variant Alleles C/A
Ancestral Allele C
Functional Annotation upstream_gene_variant.
Consequence to Transcript upstream_gene_variant(ENST00000255448; ENST00000360631; ENST00000379892)
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
Havik, B., 2012 P-value=0.168, OR (95% CI)=1.20 (0.94-1.52) in the Norwegian...... P-value=0.168, OR (95% CI)=1.20 (0.94-1.52) in the Norwegian sample; P-value=0.766, OR (95% CI)=1.05 (0.86-1.29) in the German sample; P-value=0.147, OR (95% CI)=1.15 (0.98-1.33) in the merged sample More... The marker did not show significant association with ADHD. The marker did not show significant association with ADHD. Non-significant

SNP related genes (count: 1)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 0)


SNPs in LD with rs10492555 (count: 0) View in gBrowse (chr13:36709109..36709109 )