ADHDgene Database

Hot Results

Quick Search

Keyword:
Type:

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

SNP Report

Basic Info

Name	rs2020942 dbSNP Ensembl
Location	chr17:28546914(Fwd)
Variant Alleles	C/T
Ancestral Allele	C
Functional Annotation	intron_variant.
Consequence to Transcript	intron_variant(ENST00000261707; ENST00000394821; ENST00000401766)
No. of Studies	2 (significant: 0; non-significant: 2; trend: 0)
Source	Literature-origin

SNP related studies (count: 2)

Reference	Allele Change	Risk Allele	Statistical Values	Author Comments	Result of Statistical Analysis
Brookes K, 2006	A/G		UNPHASED TDT P-value=0.195; WHAP TDT P-value=0.309 UNPHASED TDT P-value=0.195; WHAP TDT P-value=0.309	no significant association was observed no significant association was observed	Non-significant
Landaas ET, 2010	A/G		P-value=0.43, OR=0.93 in the Norwegian samples; P-value=0.61...... P-value=0.43, OR=0.93 in the Norwegian samples; P-value=0.61, OR=0.94 in the Norwegian samples; P-value=0.63, OR=0.94 in the Norwegian males More...	no significant association no significant association	Non-significant

SNP related genes (count: 1)

Literature-origin genes (count: 1)

Genes from other sources (count: 0)

SNPs in LD with rs2020942 (count: 0) View in gBrowse (chr17:28546914..28546914 )