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

SNP Report

Basic Info
Name rs790937 dbSNP Ensembl
Location chr13:50651956(Fwd)
Variant Alleles T/C
Ancestral Allele T
Functional Annotation intron_variant; nc_transcript_variant; upstream_gene_variant.
Consequence to Transcript intron_variant(ENST00000235290; ENST00000421758; ENST00000425586; ENST00000433070; ENST00000443587; ENST00000449579; ENST00000458725)
nc_transcript_variant(ENST00000235290; ENST00000421758; ENST00000425586; ENST00000433070; ENST00000443587; ENST00000449579; ENST00000458725)
upstream_gene_variant(ENST00000378180; ENST00000461527; ENST00000463474; ENST00000467721; ENST00000468168; ENST00000468522; ENST00000469754; ENST00000476738; ENST00000478860; ENST00000486895; ENST00000490577; ENST00000491341; ENST00000491615)
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 rs790937 (count: 0) View in gBrowse (chr13:50651956..50651956 )