ADHDgene Database

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Large-scale studies

Data Summary

Published Variant
- SNP: 1391
- CNV: 398
- Others: 173
Published Gene: 359
Published Region: 128
Pathway by PBA: 8
Study: 361

SNP Report

Basic Info

Name	rs3838196 dbSNP Ensembl
Location	ChrX:43702604(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(ENST00000538942; ENST00000378069; ENST00000487544; ENST00000536181) intron_variant(ENST00000538942; ENST00000378069; ENST00000487544; ENST00000536181) 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 (count: 0)

SNPs in LD with rs3838196 (count: 0) View in gBrowse (chrX:43702604..43702604 )