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	rs10761412 dbSNP Ensembl
Location	Chr9:136519590(Fwd)
Variant Alleles	T/C
Ancestral Allele	T
Functional Annotation	downstream_gene_variant; intron_variant.
Consequence to Transcript	downstream_gene_variant(ENST00000425189) intron_variant(ENST00000393056)
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
Hawi, Z., 2012	T:C	C	P-value=0.4268, X²=0.63, OR=1.11, 95% CI=0.86-1.4...... P-value=0.4268, X²=0.63, OR=1.11, 95% CI=0.86-1.43 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: 3)

Literature-origin genes (count: 1)

Genes from other sources (count: 2)

SNPs in LD with rs10761412 (count: 0) View in gBrowse (chr9:136519590..136519590 )