ADHDgene Database

Hot Results

Quick Search

Keyword:
Type:

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
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
Nyman ES, 2007			No available information. No available information.	No evidence of association was seen. No evidence of association was seen.	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 )