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

SNP Report

Basic Info
Name rs10849952 dbSNP Ensembl
Location chr12:111911285(Fwd)
Variant Alleles T/C
Ancestral Allele T
Functional Annotation intron_variant; nc_transcript_variant; NMD_transcript_variant; upstream_gene_variant.
Consequence to Transcript intron_variant(ENST00000377617; ENST00000389153; ENST00000389154; ENST00000483311; ENST00000495342; ENST00000535949; ENST00000542287; ENST00000550104; ENST00000551755; ENST00000608853)
nc_transcript_variant(ENST00000495342)
NMD_transcript_variant(ENST00000483311; ENST00000551755)
upstream_gene_variant(ENST00000482777; ENST00000550844; ENST00000550889)
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: 1)

Genes from other sources Help (count: 0)


SNPs in LD with rs10849952 (count: 0) View in gBrowse (chr12:111911285..111911285 )