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

SNP Report

Basic Info
Name rs9619267 dbSNP Ensembl
Location chr22:32886177(Fwd)
Variant Alleles C/T
Ancestral Allele C
Functional Annotation intron_variant; nc_transcript_variant; NMD_transcript_variant; non_coding_exon_variant.
Consequence to Transcript intron_variant(ENST00000266087; ENST00000382058; ENST00000397426; ENST00000420700; ENST00000425028; ENST00000484607)
nc_transcript_variant(ENST00000484607; ENST00000492535)
NMD_transcript_variant(ENST00000420700; ENST00000425028)
non_coding_exon_variant(ENST00000492535)
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 rs9619267 (count: 0) View in gBrowse (chr22:32886177..32886177 )