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	SLC6A3_exon15_G/C
Type	point mutation
Location	exon15
Related Gene	SLC6A3
No. of Study	1 (significant: 0; non-significant 1; trend: 0)

Variant related studies (count: 1)

Reference	Allele Change	Risk Allele	Statistical Values	Author Comments	Result of Statistical Analysis
Hawi Z, 2003	G/C		HHRR P-value=0.7, X²=0.15, RR=1.1 for allele1 HHRR P-value=0.7, X²=0.15, RR=1.1 for allele1	no association was detected with the markers in exons 15 no association was detected with the markers in exons 15	Non-significant