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

SNP Report

Basic Info
Name rs1044482 dbSNP Ensembl
Location chr11:71155171(Fwd)
Variant Alleles C/A/T
Ancestral Allele C
Functional Annotation intron_variant; missense_variant; splice_region_variant; synonymous_variant; upstream_gene_variant.
Polyphen Annotation: benign(ENST00000355527; ENST00000407721; ENST00000525346; ENST00000526780; ENST00000527452; ENST00000531364) | probably damaging(ENST00000529990)
SIFT Annotation: tolerated(ENST00000355527; ENST00000407721; ENST00000525346; ENST00000526780; ENST00000527452; ENST00000531364) | deleterious(ENST00000529990)
Consequence to Transcript intron_variant(ENST00000527316)
missense_variant(ENST00000355527; ENST00000407721; ENST00000525346; ENST00000526780; ENST00000527452; ENST00000531364; ENST00000529990)
splice_region_variant(ENST00000527316)
synonymous_variant(ENST00000355527; ENST00000407721; ENST00000525346; ENST00000526780; ENST00000527452; ENST00000529990; ENST00000531364)
upstream_gene_variant(ENST00000529369; ENST00000534701)
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 rs1044482 (count: 0) View in gBrowse (chr11:71155171..71155171 )