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

SNP Report

Basic Info
Name rs2693727 dbSNP Ensembl
Location chr7:129417730(Fwd)
Variant Alleles C/T
Ancestral Allele C
Functional Annotation upstream_gene_variant.
Consequence to Transcript upstream_gene_variant(ENST00000362288; ENST00000384958)
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
Sanchez-Mora, C.,2013(a) Cochran-Armitage's Trend Test P-value=0.558 Cochran-Armitage's Trend Test P-value=0.558 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. More... Non-significant

SNP related genes (count: 2)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 1)


SNPs in LD with rs2693727 (count: 9) View in gBrowse (chr7:129417730..129567692 )
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: 9)