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

SNP Report

Basic Info
Name rs10066070 dbSNP Ensembl
Location chr5:94093011(Fwd)
Variant Alleles C/T
Ancestral Allele C
Functional Annotation intron_variant; nc_transcript_variant.
Consequence to Transcript intron_variant(ENST00000312216; ENST00000429576; ENST00000505078; ENST00000508509; ENST00000514040; ENST00000515393; ENST00000573031; ENST00000573142; ENST00000573439; ENST00000574707; ENST00000575480; ENST00000577136)
nc_transcript_variant(ENST00000514040; ENST00000573031)
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 rs10066070 (count: 0) View in gBrowse (chr5:94093011..94093011 )