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

SNP Report

Basic Info
Name rs9986878 dbSNP Ensembl
Location chr7:34788062(Fwd)
Variant Alleles C/G
Ancestral Allele G
Functional Annotation downstream_gene_variant; intron_variant; nc_transcript_variant; NMD_transcript_variant; upstream_gene_variant.
Consequence to Transcript downstream_gene_variant(ENST00000432906)
intron_variant(ENST00000358772; ENST00000359791; ENST00000360581; ENST00000381539; ENST00000381542; ENST00000381544; ENST00000381553; ENST00000396095; ENST00000419766; ENST00000428922; ENST00000431669; ENST00000436945; ENST00000439852; ENST00000442669; ENST00000531252; ENST00000535640; ENST00000537560; ENST00000539747; ENST00000544556)
nc_transcript_variant(ENST00000358772; ENST00000419766; ENST00000428922; ENST00000431669; ENST00000436945; ENST00000439852; ENST00000442669; ENST00000535640; ENST00000537560; ENST00000539747; ENST00000544556)
NMD_transcript_variant(ENST00000381544; ENST00000396095)
upstream_gene_variant(ENST00000478131)
No. of Studies 0 (significant: 0; non-significant: 0; trend: 0)
Source LD-proxy

SNP related studies (count: 0)

SNP related genes (count: 4)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 3)


SNPs in LD with rs9986878 (count: 0) View in gBrowse (chr7:34788062..34788062 )