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

SNP Report

Basic Info
Name rs3796088 dbSNP Ensembl
Location chr2:234651800(Fwd)
Variant Alleles T/C
Ancestral Allele T
Functional Annotation downstream_gene_variant; intron_variant; nc_transcript_variant; NMD_transcript_variant; non_coding_exon_variant; upstream_gene_variant.
Consequence to Transcript downstream_gene_variant(ENST00000446806; ENST00000509542)
intron_variant(ENST00000305139; ENST00000344644; ENST00000354728; ENST00000373409; ENST00000373414; ENST00000373424; ENST00000373426; ENST00000373445; ENST00000373450; ENST00000406651; ENST00000446481; ENST00000450233; ENST00000480628; ENST00000482026; ENST00000484784; ENST00000608381; ENST00000609637; ENST00000609767)
nc_transcript_variant(ENST00000449667; ENST00000480628)
NMD_transcript_variant(ENST00000446481; ENST00000450233; ENST00000484784)
No. of Studies 0 (significant: 0; non-significant: 0; trend: 0)
Source LD-proxy

SNP related studies (count: 0)

SNP related genes (count: 10)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 9)

SNPs in LD with rs3796088 (count: 0) View in gBrowse (chr2:234651800..234651800 )