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

SNP Report

Basic Info
Name rs3776568 dbSNP Ensembl
Location chr5:36632611(Fwd)
Variant Alleles G/C
Ancestral Allele G
Functional Annotation downstream_gene_variant; intron_variant; nc_transcript_variant.
Consequence to Transcript downstream_gene_variant(ENST00000502864; ENST00000505202; ENST00000513646; ENST00000513903)
intron_variant(ENST00000265113; ENST00000381918; ENST00000509272; ENST00000514563)
nc_transcript_variant(ENST00000509272; ENST00000514563)
No. of Studies 1 (significant: 0; non-significant: 1; trend: 0)
Source Literature-origin

SNP related studies (count: 1)
Reference Allele Change Risk Allele Statistical Values Author Comments Result of Statistical Analysis
Turic D, 2005(a) C/G no P-value no P-value no association no association Non-significant

SNP related genes (count: 1)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 0)


SNPs in LD with rs3776568 (count: 8) View in gBrowse (chr5:36618403..36636955 )
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: 0)

LD-proxies (count: 8)