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

SNP Report

Basic Info
Name rs9545424 dbSNP Ensembl
Location chr13:36383264(Fwd)
Variant Alleles G/A
Ancestral Allele A
Functional Annotation intron_variant; upstream_gene_variant.
Consequence to Transcript intron_variant(ENST00000255448; ENST00000360631; ENST00000379893)
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=0.055, OR (95% CI)=0.75 (0.57-1.00) in the Norwegian...... P-value=0.055, OR (95% CI)=0.75 (0.57-1.00) in the Norwegian sample; P-value=0.134, OR (95% CI)=1.26 (1.02-1.55) in the German sample; P-value=0.798, OR (95% CI)=1.01 (0.86-1.20) 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 rs9545424 (count: 37) View in gBrowse (chr13:36318804..36383264 )
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: 37)