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

SNP Report

Basic Info
Name rs2010506 dbSNP Ensembl
Location chr19:19387356(Fwd)
Variant Alleles C/T
Ancestral Allele C
Functional Annotation 3_prime_UTR_variant; nc_transcript_variant; NMD_transcript_variant; non_coding_exon_variant; upstream_gene_variant.
Consequence to Transcript 3_prime_UTR_variant(ENST00000247001; ENST00000587119; ENST00000588731; ENST00000589144)
nc_transcript_variant(ENST00000591007; ENST00000592188)
NMD_transcript_variant(ENST00000587119; ENST00000588731; ENST00000589144)
non_coding_exon_variant(ENST00000591007; ENST00000592188)
upstream_gene_variant(ENST00000389363; ENST00000431465; ENST00000586064; ENST00000586107; ENST00000591001)
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: 0)

Genes from other sources Help (count: 2)


SNPs in LD with rs2010506 (count: 0) View in gBrowse (chr19:19387356..19387356 )