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

SNP Report

Basic Info
Name rs11657536 dbSNP Ensembl
Location chr17:28529242(Fwd)
Variant Alleles G/A
Ancestral Allele G
Functional Annotation intron_variant; nc_transcript_variant; NMD_transcript_variant; upstream_gene_variant.
Consequence to Transcript intron_variant(ENST00000261707; ENST00000394821; ENST00000401766; ENST00000578609; ENST00000579221)
nc_transcript_variant(ENST00000578609)
NMD_transcript_variant(ENST00000579221)
upstream_gene_variant(ENST00000581633)
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
Landaas ET, 2010 A/G P-value=0.3, OR=0.74 in the Norwegian samples; P-value=0.085...... P-value=0.3, OR=0.74 in the Norwegian samples; P-value=0.085, OR=0.48 in the Norwegian females; P-value=0.67, OR=1.2 in the Norwegian males More... no significant association no significant association Non-significant

SNP related genes (count: 1)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 0)


SNPs in LD with rs11657536 (count: 3) View in gBrowse (chr17:28428896..28529242 )
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: 3)