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

SNP Report

Basic Info
Name rs1023556 dbSNP Ensembl
Location Chr7:34696545(Fwd)
Variant Alleles C/T
Ancestral Allele T
Functional Annotation intron_variant; nc_transcript_variant; upstream_gene_variant.
Consequence to Transcript intron_variant(ENST00000439852; ENST00000419766; ENST00000358772; ENST00000539747; ENST00000431669; ENST00000537560; ENST00000535640; ENST00000399077; ENST00000544556)
nc_transcript_variant(ENST00000439852; ENST00000419766; ENST00000358772; ENST00000539747; ENST00000431669; ENST00000537560; ENST00000535640; ENST00000544556)
upstream_gene_variant(ENST00000381542; ENST00000465305; ENST00000381553; ENST00000381544; ENST00000360581; ENST00000396095; ENST00000531252; ENST00000359791; ENST00000381539)
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
Neale BM, 2010 (b) T:C GLM P-value=2.61E-05, meta-analysis P-value=0.4215 GLM P-value=2.61E-05, meta-analysis P-value=0.4215 One of the top 100 SNPs from imputed IMAGE II dataset One of the top 100 SNPs from imputed IMAGE II dataset Non-significant

SNP related genes (count: 2)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 1)


SNPs in LD with rs1023556 (count: 52) View in gBrowse (chr7:21106269..34696545 )
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: 4)

LD-proxies (count: 48)