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

SNP Report

Basic Info
Name rs9605031 dbSNP Ensembl
Location chr22:19921378(Fwd)
Variant Alleles C/T
Ancestral Allele C
Functional Annotation intron_variant; nc_transcript_variant; NMD_transcript_variant; upstream_gene_variant.
Consequence to Transcript intron_variant(ENST00000334363; ENST00000400519; ENST00000400521; ENST00000400525; ENST00000474308; ENST00000496729; ENST00000535882; LRG_417t1)
nc_transcript_variant(ENST00000474308; ENST00000496729)
upstream_gene_variant(ENST00000400518; ENST00000491939; ENST00000542719)
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 rs9605031 (count: 0) View in gBrowse (chr22:19921378..19921378 )