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

SNP Report

Basic Info
Name rs11191454 dbSNP Ensembl
Location chr10:104660004(Fwd)
Variant Alleles A/G
Ancestral Allele A
Functional Annotation intron_variant; NMD_transcript_variant.
Consequence to Transcript intron_variant(ENST00000299353; ENST00000369880)
NMD_transcript_variant(ENST00000299353)
No. of Studies 1 (significant: 1; non-significant: 0; trend: 0)
Source Literature-origin

SNP related studies (count: 1)
Reference Allele Change Risk Allele Statistical Values Author Comments Result of Statistical Analysis
PGC, 2013 A/G Five disorder meta-analysis, P-value=1.39E-08, OR (95% CI)=1...... Five disorder meta-analysis, P-value=1.39E-08, OR (95% CI)=1.13 (1.08-1.18), Heterogeneity P-value=0.32; for ADHD only, P-value=0.355 More... Significant association was observed in cross-disorder analy...... Significant association was observed in cross-disorder analysis. More... Significant

SNP related genes (count: 2)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 1)


SNPs in LD with rs11191454 (count: 42) View in gBrowse (chr10:104572276..104857523 )
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: 42)