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

SNP Report

Basic Info
Name rs7687 dbSNP Ensembl
Location chr17:44103296(Fwd)
Variant Alleles T/C
Ancestral Allele C
Functional Annotation 3_prime_UTR_variant; downstream_gene_variant.
Consequence to Transcript 3_prime_UTR_variant(ENST00000262410; ENST00000340799; ENST00000344290; ENST00000347967; ENST00000351559; ENST00000446361; ENST00000535772)
downstream_gene_variant(ENST00000262419; ENST00000334239; ENST00000393476; ENST00000415613; ENST00000420682; ENST00000431008; ENST00000432791; ENST00000571987; ENST00000572218; ENST00000572904; ENST00000574436; ENST00000574590; ENST00000575318; ENST00000576518; ENST00000576870)
No. of Studies 0 (significant: 0; non-significant: 0; trend: 0)
Source LD-proxy

SNP related studies (count: 0)

SNP related genes (count: 2)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 1)


SNPs in LD with rs7687 (count: 0) View in gBrowse (chr17:44103296..44103296 )