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

SNP Report

Basic Info

Name	rs10492555 dbSNP Ensembl
Location	Chr13:36709109(Fwd)
Variant Alleles	C/A
Ancestral Allele	C
Functional Annotation	upstream_gene_variant.
Consequence to Transcript	upstream_gene_variant(ENST00000255448; ENST00000379892; ENST00000360631)
No. of Studies	1 (significant: 0; non-significant: 1; trend: 0)
Source	Literature-origin

SNP related studies (count: 1)

Reference	Allele Change	Risk Allele	Statistical Values	Author Comments	Result of Statistical Analysis
Havik, B., 2012			P-value=0.168, OR (95% CI)=1.20 (0.94-1.52) in the Norwegian...... P-value=0.168, OR (95% CI)=1.20 (0.94-1.52) in the Norwegian sample; P-value=0.766, OR (95% CI)=1.05 (0.86-1.29) in the German sample; P-value=0.147, OR (95% CI)=1.15 (0.98-1.33) in the merged sample More...	The marker did not show significant association with ADHD. The marker did not show significant association with ADHD.	Non-significant

SNP related genes (count: 1)

Literature-origin genes (count: 1)

Genes from other sources (count: 0)

SNPs in LD with rs10492555 (count: 0) View in gBrowse (chr13:36709109..36709109 )