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

SNP Report

Basic Info
Name rs1810132 dbSNP Ensembl
Location chr17:37866005(Fwd)
Variant Alleles C/T
Ancestral Allele T
Functional Annotation downstream_gene_variant; intron_variant; nc_transcript_variant; NMD_transcript_variant; upstream_gene_variant.
Consequence to Transcript downstream_gene_variant(ENST00000578709; ENST00000584099)
intron_variant(ENST00000269571; ENST00000406381; ENST00000445658; ENST00000540042; ENST00000540147; ENST00000541774; ENST00000578199; ENST00000578373; ENST00000582648; ENST00000582788; ENST00000583038; ENST00000583391; ENST00000584450; ENST00000584601; ENST00000584908)
nc_transcript_variant(ENST00000582788; ENST00000583038; ENST00000583391; ENST00000584908)
NMD_transcript_variant(ENST00000578373; ENST00000582648)
upstream_gene_variant(ENST00000578502)
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 rs1810132 (count: 0) View in gBrowse (chr17:37866005..37866005 )