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

SNP Report

Basic Info
Name rs899393 dbSNP Ensembl
Location chr4:758366(Fwd)
Variant Alleles C/T
Ancestral Allele C
Functional Annotation downstream_gene_variant; intron_variant; nc_transcript_variant; NMD_transcript_variant; non_coding_exon_variant.
Consequence to Transcript downstream_gene_variant(ENST00000488032; ENST00000507446)
intron_variant(ENST00000362003; ENST00000430644; ENST00000440452; ENST00000470161; ENST00000503571; ENST00000505655; ENST00000521023)
nc_transcript_variant(ENST00000454037; ENST00000503571)
NMD_transcript_variant(ENST00000430644; ENST00000440452)
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: 0)

Genes from other sources Help (count: 1)

SNPs in LD with rs899393 (count: 0) View in gBrowse (chr4:758366..758366 )