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	rs9804190 dbSNP Ensembl
Location	Chr10:61839831(Fwd)
Variant Alleles	C/T
Ancestral Allele	T
Functional Annotation	downstream_gene_variant; intron_variant; upstream_gene_variant.
Consequence to Transcript	downstream_gene_variant(ENST00000395302; ENST00000508449; ENST00000510495) intron_variant(ENST00000280772; ENST00000511043; ENST00000373820; ENST00000373827; ENST00000355288; ENST00000503366) upstream_gene_variant(ENST00000365320)
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
Landaas ET, 2011		C	P-value=0.23, OR=0.89 for frequencies of the BD risk alleles...... P-value=0.23, OR=0.89 for frequencies of the BD risk alleles and genotypes in ADHD More...	did not show any association with ADHD did not show any 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 rs9804190 (count: 0) View in gBrowse (chr10:61839831..61839831 )