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	rs2678787 dbSNP Ensembl
Location	Chr18:28182328(Fwd)
Variant Alleles	C/T
Ancestral Allele	T
No. of Studies	2 (significant: 0; non-significant: 2; trend: 0)
Source	Literature-origin

SNP related studies (count: 2)

Reference	Allele Change	Risk Allele	Statistical Values	Author Comments	Result of Statistical Analysis
Lantieri F, 2010	C:T		Binomial P-value=0.52, OR=1 for whole sample; Binomial P-val...... Binomial P-value=0.52, OR=1 for whole sample; Binomial P-value=0.58, OR=1.02 for C-subtype More...	no significant association no significant association	Non-significant
Neale BM, 2008	C:T		Corrected TDT P-value=6.36E-05 (OR=0.7228) Corrected TDT P-value=6.36E-05 (OR=0.7228)	One of top 25 results in corrected TDT test One of top 25 results in corrected TDT test	Non-significant

SNP related genes (count: 0)

SNPs in LD with rs2678787 (count: 0) View in gBrowse (chr18:28182328..28182328 )