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	SLC6A2_exon5_848C/T
Type	point mutation
Location	exon 5
Related Gene	SLC6A2
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
Hahn MK, 2009	C:T			non-synonymous SNP in coding region of candidate gene SLC6A2 non-synonymous SNP in coding region of candidate gene SLC6A2	Trend