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

SNP Report

Basic Info
Name rs3838196 dbSNP Ensembl
Location chrX:43702652(Fwd)
Variant Alleles -/CA
Functional Annotation downstream_gene_variant; feature_truncation; intron_variant; nc_transcript_variant.
Consequence to Transcript downstream_gene_variant(ENST00000468431)
feature_truncation(ENST00000378069; ENST00000487544; ENST00000536181; ENST00000538942)
intron_variant(ENST00000378069; ENST00000487544; ENST00000536181; ENST00000538942)
nc_transcript_variant(ENST00000487544)
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
Domschke K, 2005 allelic TDT P-value=0.56, LRS=5.8, df=7 allelic TDT P-value=0.56, LRS=5.8, df=7 did not show any significant distortion in the transmission ...... did not show any significant distortion in the transmission to ADHD cases More... Non-significant

SNP related genes (count: 1)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 0)


SNPs in LD with rs3838196 (count: 0) View in gBrowse (chrX:43702652..43702652 )