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

SNP Report

Basic Info
Name rs2299110 dbSNP Ensembl
Location Chr7:28759900(Fwd)
Variant Alleles C/T
Ancestral Allele C
Functional Annotation intron_variant; nc_transcript_variant; upstream_gene_variant.
Consequence to Transcript intron_variant(ENST00000396299; ENST00000409603; ENST00000396300; ENST00000468391; ENST00000461921; ENST00000426500; ENST00000396298; ENST00000357727; ENST00000484383)
nc_transcript_variant(ENST00000468391; ENST00000461921; ENST00000484383)
upstream_gene_variant(ENST00000468813)
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 rs2299110 (count: 1) View in gBrowse (chr7:28759900..28762963 )
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)