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

SNP Report

Basic Info
Name rs3813929 dbSNP Ensembl
Location chrX:113818520(Fwd)
Variant Alleles C/T
Ancestral Allele C
Functional Annotation upstream_gene_variant.
Consequence to Transcript upstream_gene_variant(ENST00000276198; ENST00000371950; ENST00000371951)
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
Xu X, 2009(a) C-759T TDT P-value=0.384, OR=1.2 TDT P-value=0.384, OR=1.2 no significant association with ADHD was found no significant association with ADHD was found Non-significant
Li J, 2006(a) C/T TDT P-value=0.045, X2=4.009 in ADHD; TDT P-value=...... TDT P-value=0.045, X2=4.009 in ADHD; TDT P-value=0.175, X2=1.841 in ADHD-C; TDT P-value=0.298, X2=1.085 in ADHD-I More... a preferential transmission of the C allele to ADHD probands a preferential transmission of the C allele to ADHD probands Significant

SNP related genes (count: 1)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 0)


SNPs in LD with rs3813929 (count: 41) View in gBrowse (chrX:113776160..114000273 )
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: 41)