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	LPHN3_1869-13T>C
Type	point mutation
Location	intron
Related Gene	LPHN3
No. of Study	1 (significant: 0; non-significant 0; trend: 1)

Variant related studies (count: 1)

Reference	Allele Change	Risk Allele	Statistical Values	Author Comments	Result of Statistical Analysis
Domene S, 2011	c.1869-13T>C		Obs_HET/Pred_HET=176/176 Obs_HET/Pred_HET=176/176	neither susceptibility nor protective haplotype alleles are ...... neither susceptibility nor protective haplotype alleles are associated with obviously significant coding region changes, or canonical splice site alterations More...	Trend