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

SNP Report

Basic Info
Name rs1491850 dbSNP Ensembl
Location chr11:27749725(Fwd)
Variant Alleles T/C
Ancestral Allele T
Functional Annotation intron_variant; nc_transcript_variant.
Consequence to Transcript intron_variant(ENST00000530663)
nc_transcript_variant(ENST00000530663)
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, 2008 genotypic P-value=0.11; genotypic P-value=0.05, OR=1.42 (1.0...... genotypic P-value=0.11; genotypic P-value=0.05, OR=1.42 (1.00-2.02) in dominant model; genotypic P-value=0.18 in recessive model; allelic P-value=0.04, OR=1.26 (1.01-1.59) in Adults; genotypic P-value=0.12; genotypic P-value=0.057 in dominant model; genotypic P-value=0.15 in recessive model; allelic P-value=0.037, OR=1.24 (1.01-1.51) in Children More... provided evidence of association with adulthood and childhoo...... provided evidence of association with adulthood and childhood ADHD More... Significant

SNP related genes (count: 0)

SNPs in LD with rs1491850 (count: 17) View in gBrowse (chr11:27572337..27749725 )
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: 17)