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

SNP Report

Basic Info
Name rs1124491 dbSNP Ensembl
Location chr11:113282090(Fwd)
Variant Alleles G/A
Ancestral Allele G
Functional Annotation downstream_gene_variant; intron_variant; nc_transcript_variant.
Consequence to Transcript downstream_gene_variant(ENST00000535984; ENST00000539420; ENST00000540600)
intron_variant(ENST00000346454; ENST00000355319; ENST00000362072; ENST00000538967; ENST00000542968; ENST00000544518; ENST00000546284)
nc_transcript_variant(ENST00000546284)
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
Nyman ES, 2007 Logistic regression for single markers: Males: P-value=0.017...... Logistic regression for single markers: Males: P-value=0.0174, OR=2.08, 95%CI=1.14-3.80 for 22/12vs.11 More... Association was observed in males. No evidence of associatio...... Association was observed in males. No evidence of association was seen in the complete sample or in females. More... Significant

SNP related genes (count: 1)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 0)


SNPs in LD with rs1124491 (count: 45) View in gBrowse (chr11:113249725..113387809 )
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: 45)