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	MTNR1A_C/G_Y170X
Type	point mutation
Related Gene	MTNR1A
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
Chaste P, 2011	C/G		no data no data	modify the protein sequence; but no significant enrichment; ...... modify the protein sequence; but no significant enrichment; this mutation was predicted to cause severe functional alterations and were detected in two independent patients with ADHD, but not in the geographically matched comparison group. More...	Significant