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

SNP Report

Basic Info
Name rs1150222 dbSNP Ensembl
Location chr11:113846872(Fwd)
Variant Alleles G/T
Ancestral Allele G
Functional Annotation intron_variant; NMD_transcript_variant; upstream_gene_variant.
Consequence to Transcript intron_variant(ENST00000355556; ENST00000375498; ENST00000504030; ENST00000506841; ENST00000510849; ENST00000535865)
NMD_transcript_variant(ENST00000510849)
upstream_gene_variant(ENST00000299961; ENST00000502622)
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
Ribases M, 2009(b) Case-control test: lowest P-value=0.012 for genotype analysi...... Case-control test: lowest P-value=0.012 for genotype analysis, P-value=0.051 for allele analysis in adult inattentive ADHD. More... no significance after correcting for multiple comparisons no significance after correcting for multiple comparisons Significant

SNP related genes (count: 1)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 0)


SNPs in LD with rs1150222 (count: 10) View in gBrowse (chr11:113839272..113863131 )
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: 10)