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

SNP Report

Basic Info
Name rs165599 dbSNP Ensembl
Location chr22:19956781(Fwd)
Variant Alleles G/A
Ancestral Allele G
Functional Annotation 3_prime_UTR_variant; downstream_gene_variant.
Consequence to Transcript 3_prime_UTR_variant(ENST00000361682; ENST00000449653)
downstream_gene_variant(ENST00000207636; ENST00000263207; ENST00000344269; ENST00000401994; ENST00000403184; ENST00000403710; ENST00000406259; ENST00000406520; ENST00000406522; ENST00000407537; ENST00000412786; ENST00000428707; ENST00000480792; ENST00000493893; ENST00000495096)
No. of Studies 2 (significant: 1; non-significant: 1; trend: 0)
Source Literature-origin

SNP related studies (count: 2)
Reference Allele Change Risk Allele Statistical Values Author Comments Result of Statistical Analysis
Turic D, 2005(b) G/A allelic TRANSMIT P-value (10,000 simulations)=0.71, X2<...... allelic TRANSMIT P-value (10,000 simulations)=0.71, X2=0.154 More... did not show preferential transmission of any allele did not show preferential transmission of any allele Non-significant
Michaelovsky E, 2008 A/G P-value=0.02, X2(1)=5.44 P-value=0.02, X2(1)=5.44 showed significant association with ADHD showed significant association with ADHD Significant

SNP related genes (count: 2)

Literature-origin genes (count: 2)

Genes from other sources Help (count: 0)

SNPs in LD with rs165599 (count: 0) View in gBrowse (chr22:19956781..19956781 )