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

SNP Report

Basic Info
Name rs6965643 dbSNP Ensembl
Location chr7:129407564(Fwd)
Variant Alleles A/G
Ancestral Allele A
Functional Annotation downstream_gene_variant.
Consequence to Transcript downstream_gene_variant(ENST00000385255)
No. of Studies 1 (significant: 1; non-significant: 0; trend: 0)
Source Literature-origin

SNP related studies (count: 1)
Reference Allele Change Risk Allele Statistical Values Author Comments Result of Statistical Analysis
Sanchez-Mora, C.,2013(a) Cochran-Armitage's Trend Test P-value=0.029 (OR=1.31;95%CI=1...... Cochran-Armitage's Trend Test P-value=0.029 (OR=1.31;95%CI=1.02-1.66) More... In the single-marker analysis,the comparison of genotype fre...... In the single-marker analysis,the comparison of genotype frequencies between the whole ADHD sample and the control group showed no significant differences. However, this SNP located downstream from miR-96 displayed nominal association with ADHD without comorbid SUD. Consistently, this difference remained significant for rs6965643 when ADHD with neither SUD nor disruptive behavior disorders was compared with the control group. More... Significant

SNP related genes (count: 2)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 1)

SNPs in LD with rs6965643 (count: 0) View in gBrowse (chr7:129407564..129407564 )