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

SNP Report

Basic Info
Name rs4666807 dbSNP Ensembl
Location Chr2:182907386(Fwd)
Variant Alleles G/C
Ancestral Allele G
Functional Annotation intron_variant; nc_transcript_variant.
Consequence to Transcript intron_variant(ENST00000495820; ENST00000464264; ENST00000475249; ENST00000486067; ENST00000465612; ENST00000280295; ENST00000479855; ENST00000490645; ENST00000409137; ENST00000409702; ENST00000452904)
nc_transcript_variant(ENST00000464264; ENST00000495820; ENST00000475249; ENST00000486067; ENST00000479855; ENST00000465612; ENST00000490645)
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 rs4666807 (count: 1) View in gBrowse (chr2:182901257..182907386 )
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)