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	rs7990263 dbSNP Ensembl
Location	Chr13:36461216(Fwd)
Variant Alleles	A/C
Ancestral Allele	A
Functional Annotation	intron_variant.
Consequence to Transcript	intron_variant(ENST00000379892; ENST00000360631; ENST00000255448)
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=0.107, OR (95% CI)=0.85 (0.70-1.03) in the Norwegian...... P-value=0.107, OR (95% CI)=0.85 (0.70-1.03) in the Norwegian sample; P-value=0.714, OR (95% CI)=1.02 (0.88-1.20) in the German sample; P-value=0.481, OR (95% CI)=0.93 (0.83-1.05) 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 rs7990263 (count: 0) View in gBrowse (chr13:36461216..36461216 )