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

SNP Report

Basic Info
Name rs1056484 dbSNP Ensembl
Location chr22:32908738(Fwd)
Variant Alleles T/C
Ancestral Allele T
Functional Annotation 3_prime_UTR_variant; downstream_gene_variant.
Consequence to Transcript 3_prime_UTR_variant(ENST00000332840; ENST00000358763)
downstream_gene_variant(ENST00000461446; ENST00000467095; ENST00000483062)
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
Makkar R, 2007 C/T TDT P-value=0.651, X2=0.205 TDT P-value=0.651, X2=0.205 no significant biased transmission for any of the alleles of...... no significant biased transmission for any of the alleles of the polymorphism was observed using the TDT More... Non-significant

SNP related genes (count: 1)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 0)


SNPs in LD with rs1056484 (count: 7) View in gBrowse (chr22:32886177..32913733 )
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: 7)