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

SNP Report

Basic Info
Name rs6295 dbSNP Ensembl
Location chr5:63258565(Fwd)
Variant Alleles C/G
Ancestral Allele G
Functional Annotation intron_variant; nc_transcript_variant; upstream_gene_variant.
Consequence to Transcript intron_variant(ENST00000502882)
nc_transcript_variant(ENST00000502882)
upstream_gene_variant(ENST00000323865; ENST00000506598)
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
Park, Y. H.,2013 C/G allelic chi-square tests P-value=0.128 (OR=1.36; 95%CI=0.92-...... allelic chi-square tests P-value=0.128 (OR=1.36; 95%CI=0.92-2.03; X2=1.52); genotypic chi-square tests P-value=0.081 (OR=2.64; 95%CI=0.89-7.85; X2=1.75). More... No significant difference was reported in this study. No significant difference was reported in this study. Non-significant
Shim SH, 2010 G/C Multivariate model for genotype 'GG' P-value=0.834, OR=0.88;...... Multivariate model for genotype 'GG' P-value=0.834, OR=0.88; genotype 'CG' OR=1; genotype 'CC' P-value=0.039, OR=2.12; Multivariate model for allele, 'G' OR=1; allele 'C' P-value=0.026, OR=1.79 More... statistically significant differences in the genotype distri...... statistically significant differences in the genotype distributions and allele frequencies and the homozygous allele C frequency was significantly higher in ADHD patients than in controls More... Significant

SNP related genes (count: 1)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 0)


SNPs in LD with rs6295 (count: 0) View in gBrowse (chr5:63258565..63258565 )