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_exon9_1342A>G
Type	point mutation
Location	exon 9
Related Gene	SLC6A3
No. of Study	2 (significant: 0; non-significant 2; trend: 0)

Variant related studies (count: 2)

Reference	Allele Change	Risk Allele	Statistical Values	Author Comments	Result of Statistical Analysis
Hawi Z, 2003	A/G		HHRR P-value=0.22, X²=1.45, RR=1.18 for allele2 HHRR P-value=0.22, X²=1.45, RR=1.18 for allele2	no association was detected with the markers in exons 9 no association was detected with the markers in exons 9	Non-significant
Barr CL, 2001(a)	A/G		allelic TDT two-sided P-value=0.119, X^{2^=2.419} allelic TDT two-sided P-value=0.119, X^{2^=2.419}	the TDT was not significant for any allele of the polymorphi...... the TDT was not significant for any allele of the polymorphism More...	Non-significant