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

SNP Report

Basic Info
Name rs9909362 dbSNP Ensembl
Location chr17:21215204(Fwd)
Variant Alleles C/T
Ancestral Allele C
Functional Annotation intron_variant; nc_transcript_variant; NMD_transcript_variant; non_coding_exon_variant; upstream_gene_variant.
Consequence to Transcript intron_variant(ENST00000316920; ENST00000342679; ENST00000361818; ENST00000395491; ENST00000496046)
NMD_transcript_variant(ENST00000395491; ENST00000496046)
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 rs9909362 (count: 0) View in gBrowse (chr17:21215204..21215204 )