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

SNP Report

Basic Info
Name rs4969391 dbSNP Ensembl
Location chr17:79089590(Fwd)
Variant Alleles A/G
Ancestral Allele A
Functional Annotation 3_prime_UTR_variant; downstream_gene_variant; missense_variant; nc_transcript_variant; non_coding_exon_variant.
Polyphen Annotation: benign(ENST00000572498; ENST00000321300; ENST00000392411; ENST00000428708)
SIFT Annotation: deleterious(ENST00000572498) | tolerated(ENST00000321300; ENST00000392411; ENST00000428708)
Consequence to Transcript 3_prime_UTR_variant(ENST00000435091; ENST00000575245)
downstream_gene_variant(ENST00000326724; ENST00000374792; ENST00000417379; ENST00000570932; ENST00000573469)
missense_variant(ENST00000572498; ENST00000321300; ENST00000392411; ENST00000428708)
nc_transcript_variant(ENST00000576225)
non_coding_exon_variant(ENST00000576225)
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: 1)

Genes from other sources Help (count: 1)


SNPs in LD with rs4969391 (count: 0) View in gBrowse (chr17:79089590..79089590 )