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

SNP Report

Basic Info
Name rs1064395 dbSNP Ensembl
Location chr19:19361735(Fwd)
Variant Alleles G/A
Ancestral Allele G
Functional Annotation 3_prime_UTR_variant; downstream_gene_variant; intron_variant.
Consequence to Transcript 3_prime_UTR_variant(ENST00000252575)
downstream_gene_variant(ENST00000291481; ENST00000585410; ENST00000586064; ENST00000588231)
intron_variant(ENST00000538881)
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
Schimmelmann, B. G.,2013 Nominal two-sided P-value=0.087 (OR=1.91;95%CI=0.97-1.45) Nominal two-sided P-value=0.087 (OR=1.91;95%CI=0.97-1.45) We found no significant association of childhood ADHD with s...... We found no significant association of childhood ADHD with single BD risk alleles surviving adjustment for multiple testing. Only for the two coding SNPs in NCAN and BRE, we observed a consistent risk allele pattern across both control group comparisons. More... Non-significant

SNP related genes (count: 2)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 1)


SNPs in LD with rs1064395 (count: 28) View in gBrowse (chr19:19357685..19560063 )
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: 28)