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	rs916455 dbSNP Ensembl
Location	Chr11:636929(Fwd)
Variant Alleles	C/T
Ancestral Allele	C
Functional Annotation	upstream_gene_variant.
Consequence to Transcript	upstream_gene_variant(ENST00000176183; ENST00000528733)
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
Nyman ES, 2007			No available information. No available information.	No evidence of association was seen. No evidence of association was seen.	Non-significant
Yang JW, 2008	C/T		Fisher's exact test, P-value=0.838 and X² =0.013,...... Fisher's exact test, P-value=0.838 and X² =0.013, P-value=0.910 for genotypes and alleles More...	no evidence for association no evidence for association	Non-significant

SNP related genes (count: 1)

Literature-origin genes (count: 1)

Genes from other sources (count: 0)

SNPs in LD with rs916455 (count: 0) View in gBrowse (chr11:636929..636929 )