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

SNP Report

Basic Info
Name rs220379 dbSNP Ensembl
Location chr16:3339435(Fwd)
Variant Alleles G/C
Ancestral Allele C
Functional Annotation 3_prime_UTR_variant; 5_prime_UTR_variant; downstream_gene_variant; missense_variant; upstream_gene_variant.
Polyphen Annotation: benign(ENST00000219069; ENST00000574253)
SIFT Annotation: tolerated(ENST00000219069; ENST00000574253)
Consequence to Transcript 3_prime_UTR_variant(ENST00000575823)
downstream_gene_variant(ENST00000572748; ENST00000573578)
missense_variant(ENST00000219069; ENST00000574253)
upstream_gene_variant(ENST00000574674; ENST00000575332)
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 rs220379 (count: 0) View in gBrowse (chr16:3339435..3339435 )