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

SNP Report

Basic Info
Name rs7679050 dbSNP Ensembl
Location Chr4:20707821(Fwd)
Variant Alleles G/A
Ancestral Allele G
Functional Annotation NMD_transcript_variant; downstream_gene_variant; intron_variant; upstream_gene_variant.
Consequence to Transcript NMD_transcript_variant(ENST00000508952; ENST00000506702; ENST00000506951; ENST00000471979; ENST00000467997; ENST00000503747)
downstream_gene_variant(ENST00000509625; ENST00000511160; ENST00000505160; ENST00000510700; ENST00000508753)
intron_variant(ENST00000510051; ENST00000513861; ENST00000502374; ENST00000538990; ENST00000507634; ENST00000503585; ENST00000508952; ENST00000506702; ENST00000504630; ENST00000513590; ENST00000506951; ENST00000502938; ENST00000471979; ENST00000511089; ENST00000467997; ENST00000514292; ENST00000515339; ENST00000513459; ENST00000514663; ENST00000360916; ENST00000444671; ENST00000509469; ENST00000514485; ENST00000295290; ENST00000503747; ENST00000506745)
upstream_gene_variant(ENST00000506457)
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 rs7679050 (count: 1) View in gBrowse (chr4:20707821..20730780 )
The LD data used here is based on HapMap rel#27. LD SNP pairs were selected with a threshold r2>=0.8.

Literature-origin SNPs (count: 1)

LD-proxies (count: 0)