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

SNP Report

Basic Info
Name rs4494608 dbSNP Ensembl
Location chr17:28488791(Fwd)
Variant Alleles C/T
Ancestral Allele T
Functional Annotation intron_variant; nc_transcript_variant; NMD_transcript_variant.
Consequence to Transcript intron_variant(ENST00000247026; ENST00000394826; ENST00000467446; ENST00000475652; ENST00000540900; ENST00000577289; ENST00000580103; ENST00000581048; ENST00000584154; ENST00000584317; ENST00000585881; ENST00000588614; ENST00000589608)
nc_transcript_variant(ENST00000467446; ENST00000540900; ENST00000577289; ENST00000581048)
NMD_transcript_variant(ENST00000394826; ENST00000475652; ENST00000584154; ENST00000584317; ENST00000589608)
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 rs4494608 (count: 0) View in gBrowse (chr17:28488791..28488791 )