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

SNP Report

Basic Info
Name rs2229193 dbSNP Ensembl
Location chr16:9943666(Fwd)
Variant Alleles C/T
Ancestral Allele C
Functional Annotation downstream_gene_variant; synonymous_variant.
Consequence to Transcript downstream_gene_variant(ENST00000566683)
synonymous_variant(ENST00000330684; ENST00000396573; ENST00000396575; ENST00000404927; ENST00000535259; ENST00000562109)
No. of Studies 2 (significant: 0; non-significant: 2; trend: 0)
Source Literature-origin

SNP related studies (count: 2)
Reference Allele Change Risk Allele Statistical Values Author Comments Result of Statistical Analysis
Park, S.,2013 G/A allelic P-value=0.499 (Cohen`s w=0.03;X2=0.46);ge...... allelic P-value=0.499 (Cohen`s w=0.03;X2=0.46);genotypic P-value=0.421 (Cohen`s w=0.07;X2=1.73);TDT P-value=0.262,Cohen`s w=0.07, X2=1.26. More... This SNP was not significant associated with ADHD This SNP was not significant associated with ADHD Non-significant
Nyman ES, 2007 No available information. No available information. No evidence of association was seen. No evidence of association was seen. Non-significant

SNP related genes (count: 1)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 0)

SNPs in LD with rs2229193 (count: 0) View in gBrowse (chr16:9943666..9943666 )