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

Other Variant Report

Basic Info

Name	NOS1_Ex1f_VNTR
Type	VNTR
Location	33 bp downstream of the TATA box
Related Gene	NOS1
No. of Study	1 (significant: 1; non-significant 0; trend: 0)

Variant related studies (count: 1)

Reference	Allele Change	Risk Allele	Statistical Values	Author Comments	Result of Statistical Analysis
Reif A, 2009			Case-control test P-value=0.002 for aADHD group; TDT P-value...... Case-control test P-value=0.002 for aADHD group; TDT P-value=0.16 for fADHD group; multivariate logistic regression analysis P-value=0.04 for forensic group. More...	short NOS1 Ex1f VNTR alleles were associated with aADHD short NOS1 Ex1f VNTR alleles were associated with aADHD	Significant