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

SNP Report

Basic Info
Name rs3842753 dbSNP Ensembl
Location chr11:2181060(Fwd)
Variant Alleles T/G
Ancestral Allele T
Functional Annotation 3_prime_UTR_variant; downstream_gene_variant; intron_variant; missense_variant; NMD_transcript_variant; upstream_gene_variant.
Polyphen Annotation: benign(ENST00000421783)
SIFT Annotation: tolerated(ENST00000421783)
Consequence to Transcript 3_prime_UTR_variant(ENST00000250971; ENST00000381330; ENST00000397262)
downstream_gene_variant(ENST00000333684; ENST00000352909; ENST00000381175; ENST00000381178; ENST00000512523)
intron_variant(ENST00000356578; ENST00000397270)
missense_variant(ENST00000421783)
NMD_transcript_variant(ENST00000356578)
upstream_gene_variant(ENST00000476874; ENST00000481781)
No. of Studies 1 (significant: 0; non-significant: 1; trend: 0)
Source Literature-origin

SNP related studies (count: 1)
Reference Allele Change Risk Allele Statistical Values Author Comments Result of Statistical Analysis
Nyman ES, 2007 No available information. No available information. No evidence of association was seen. No evidence of association was seen. Non-significant

SNP related genes (count: 3)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 2)


SNPs in LD with rs3842753 (count: 0) View in gBrowse (chr11:2181060..2181060 )