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

SNP Report

Basic Info
Name rs944873 dbSNP Ensembl
Location Chr20:10166398(Fwd)
Variant Alleles C/A
Ancestral Allele C
Functional Annotation intron_variant; nc_transcript_variant; non_coding_exon_variant.
Consequence to Transcript intron_variant(ENST00000426491; ENST00000424931; ENST00000451151; ENST00000421143; ENST00000453544)
nc_transcript_variant(ENST00000426491; ENST00000424931; ENST00000451151; ENST00000421143; ENST00000453544; ENST00000458004)
non_coding_exon_variant(ENST00000458004)
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 rs944873 (count: 1) View in gBrowse (chr20:10166398..10193294 )
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)