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

SNP Report

Basic Info
Name rs1058808 dbSNP Ensembl
Location chr17:37884037(Fwd)
Variant Alleles C/G
Ancestral Allele C
Functional Annotation 3_prime_UTR_variant; downstream_gene_variant; missense_variant; NMD_transcript_variant; upstream_gene_variant.
Polyphen Annotation: benign(ENST00000269571; ENST00000406381; ENST00000540147; ENST00000584601) | possibly damaging(ENST00000445658; ENST00000541774)
SIFT Annotation: tolerated(ENST00000269571; ENST00000406381; ENST00000540147; ENST00000584601; ENST00000445658; ENST00000541774)
Consequence to Transcript 3_prime_UTR_variant(ENST00000578373; ENST00000584450)
downstream_gene_variant(ENST00000394231; ENST00000469568; ENST00000474210; ENST00000498164; ENST00000577810; ENST00000578630; ENST00000580074; ENST00000580969; ENST00000582818; ENST00000582963; ENST00000583038)
missense_variant(ENST00000269571; ENST00000406381; ENST00000540147; ENST00000584601; ENST00000445658; ENST00000541774)
NMD_transcript_variant(ENST00000578373)
upstream_gene_variant(ENST00000584888)
No. of Studies 0 (significant: 0; non-significant: 0; trend: 0)
Source LD-proxy

SNP related studies (count: 0)

SNP related genes (count: 3)

Literature-origin genes (count: 0)

Genes from other sources Help (count: 3)


SNPs in LD with rs1058808 (count: 0) View in gBrowse (chr17:37884037..37884037 )