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

SNP Report

Basic Info
Name rs3776585 dbSNP Ensembl
Location Chr5:36668022(Fwd)
Variant Alleles A/G
Ancestral Allele A
Functional Annotation intron_variant; nc_transcript_variant; upstream_gene_variant.
Consequence to Transcript intron_variant(ENST00000514563; ENST00000265113; ENST00000510740; ENST00000427100; ENST00000509272; ENST00000381918)
nc_transcript_variant(ENST00000514563; ENST00000510740; ENST00000509272)
upstream_gene_variant(ENST00000505376)
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) A/G P-value=0.20 for pooled genotyping P-value=0.20 for pooled genotyping not significantly associated with ADHD not significantly associated with ADHD Non-significant

SNP related genes (count: 1)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 0)


SNPs in LD with rs3776585 (count: 1) View in gBrowse (chr5:36667579..36668022 )
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: 1)