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	rs7682295 dbSNP Ensembl
Location	Chr4:3765225(Fwd)
Variant Alleles	T/G
Ancestral Allele	T
Functional Annotation	upstream_gene_variant.
Consequence to Transcript	upstream_gene_variant(ENST00000511928; ENST00000330055; ENST00000509482)
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
Guan L, 2009			single SNP association analyses: Nominal P-value=0.036, Empi...... single SNP association analyses: Nominal P-value=0.036, Empirical P-value=0.105 for ADHD \| Nominal P-value=0.011, Empirical P-value=0.042 for ADHD-C More...	achieve nominal significance for ADHD and ADHD-C, also empir...... achieve nominal significance for ADHD and ADHD-C, also empirical significante for ADHD-C More...	Significant

SNP related genes (count: 1)

Literature-origin genes (count: 1)

Genes from other sources (count: 0)

SNPs in LD with rs7682295 (count: 0) View in gBrowse (chr4:3765225..3765225 )