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

SNP Report

Basic Info
Name rs7797772 dbSNP Ensembl
Location Chr7:50460208(Fwd)
Variant Alleles G/A
Ancestral Allele G
Functional Annotation intron_variant; nc_transcript_variant.
Consequence to Transcript intron_variant(ENST00000346667; ENST00000440768; ENST00000438033; ENST00000343574; ENST00000426121; ENST00000331340; ENST00000349824; ENST00000439701; ENST00000357364; ENST00000471793; ENST00000359197)
nc_transcript_variant(ENST00000471793)
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 rs7797772 (count: 2) View in gBrowse (chr7:50460208..50607206 )
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: 2)

LD-proxies (count: 0)