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

SNP Report

Basic Info
Name rs4969381 dbSNP Ensembl
Location chr17:79054676(Fwd)
Variant Alleles C/T
Ancestral Allele C
Functional Annotation downstream_gene_variant; intron_variant; nc_transcript_variant; NMD_transcript_variant; upstream_gene_variant.
Consequence to Transcript downstream_gene_variant(ENST00000570913)
intron_variant(ENST00000321280; ENST00000321300; ENST00000392411; ENST00000428708; ENST00000435091; ENST00000571530; ENST00000572073; ENST00000572329; ENST00000572918; ENST00000573017; ENST00000573659; ENST00000573677; ENST00000573894; ENST00000574804; ENST00000575245; ENST00000575712; ENST00000575750; ENST00000575958; ENST00000575989; ENST00000576364; ENST00000576470)
nc_transcript_variant(ENST00000573017; ENST00000573894; ENST00000576364; ENST00000576470)
NMD_transcript_variant(ENST00000572329; ENST00000574804; ENST00000575750)
upstream_gene_variant(ENST00000574688; ENST00000576225; ENST00000577097)
No. of Studies 0 (significant: 0; non-significant: 0; trend: 0)
Source LD-proxy

SNP related studies (count: 0)

SNP related genes (count: 1)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 0)


SNPs in LD with rs4969381 (count: 0) View in gBrowse (chr17:79054676..79054676 )