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

SNP Report

Basic Info
Name rs260462 dbSNP Ensembl
Location chr19:58774071(Fwd)
Variant Alleles A/G
Ancestral Allele G
Functional Annotation 3_prime_UTR_variant; downstream_gene_variant; intron_variant; missense_variant; nc_transcript_variant; NMD_transcript_variant; upstream_gene_variant.
Polyphen Annotation: benign(ENST00000269829; ENST00000415203; ENST00000596652; ENST00000599953; ENST00000600044; ENST00000600220)
SIFT Annotation: tolerated(ENST00000269829; ENST00000415203; ENST00000596652; ENST00000599953; ENST00000600044; ENST00000600220)
Consequence to Transcript 3_prime_UTR_variant(ENST00000596677; ENST00000596825; ENST00000599227)
downstream_gene_variant(ENST00000594384; ENST00000598880)
intron_variant(ENST00000595981; ENST00000596929; ENST00000597230; ENST00000600029)
missense_variant(ENST00000269829; ENST00000415203; ENST00000596652; ENST00000599953; ENST00000600044; ENST00000600220)
nc_transcript_variant(ENST00000597230)
NMD_transcript_variant(ENST00000596677; ENST00000600029)
upstream_gene_variant(ENST00000595301)
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 rs260462 (count: 0) View in gBrowse (chr19:58774071..58774071 )