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

SNP Report

Basic Info
Name rs9194 dbSNP Ensembl
Location chr1:204991770(Fwd)
Variant Alleles C/T
Ancestral Allele C
Functional Annotation 3_prime_UTR_variant; downstream_gene_variant; nc_transcript_variant; non_coding_exon_variant.
Consequence to Transcript 3_prime_UTR_variant(ENST00000338515; ENST00000338586; ENST00000339876; ENST00000360049; ENST00000367169; ENST00000367170; ENST00000367171; ENST00000367172; ENST00000401399; ENST00000539706)
downstream_gene_variant(ENST00000367173; ENST00000404076; ENST00000404907; ENST00000425360; ENST00000430393; ENST00000447819; ENST00000503221)
nc_transcript_variant(ENST00000495396)
non_coding_exon_variant(ENST00000495396)
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 rs9194 (count: 0) View in gBrowse (chr1:204991770..204991770 )