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

SNP Report

Basic Info
Name rs7669 dbSNP Ensembl
Location chr13:28009851(Fwd)
Variant Alleles G/A/C
Ancestral Allele G
Functional Annotation downstream_gene_variant; missense_variant; nc_transcript_variant; non_coding_exon_variant; synonymous_variant; upstream_gene_variant.
Polyphen Annotation: benign(ENST00000381116; ENST00000381120; ENST00000405591; ENST00000431572)
SIFT Annotation: tolerated(ENST00000381116; ENST00000381120; ENST00000405591; ENST00000431572)
Consequence to Transcript downstream_gene_variant(ENST00000381140; ENST00000419181; ENST00000435781; ENST00000438571; ENST00000439403; ENST00000460973; ENST00000464753; ENST00000466776; ENST00000470606; ENST00000471771; ENST00000483903; ENST00000484342; ENST00000485650; ENST00000485959; ENST00000493719; ENST00000493903)
missense_variant(ENST00000381116; ENST00000381120; ENST00000405591; ENST00000431572)
nc_transcript_variant(ENST00000461838; ENST00000482655)
non_coding_exon_variant(ENST00000461838; ENST00000482655)
synonymous_variant(ENST00000381116; ENST00000381120; ENST00000405591; ENST00000431572)
upstream_gene_variant(ENST00000366409)
No. of Studies 0 (significant: 0; non-significant: 0; trend: 0)
Source LD-proxy

SNP related studies (count: 0)

SNP related genes (count: 2)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 1)


SNPs in LD with rs7669 (count: 0) View in gBrowse (chr13:28009851..28009851 )