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

SNP Report

Basic Info
Name rs7990263 dbSNP Ensembl
Location chr13:36461216(Fwd)
Variant Alleles A/C
Ancestral Allele A
Functional Annotation intron_variant.
Consequence to Transcript intron_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=0.107, OR (95% CI)=0.85 (0.70-1.03) in the Norwegian...... P-value=0.107, OR (95% CI)=0.85 (0.70-1.03) in the Norwegian sample; P-value=0.714, OR (95% CI)=1.02 (0.88-1.20) in the German sample; P-value=0.481, OR (95% CI)=0.93 (0.83-1.05) 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 rs7990263 (count: 0) View in gBrowse (chr13:36461216..36461216 )