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	rs6295 dbSNP Ensembl
Location	Chr5:63258565(Fwd)
Variant Alleles	C/G
Ancestral Allele	G
Functional Annotation	intron_variant; nc_transcript_variant; upstream_gene_variant.
Consequence to Transcript	intron_variant(ENST00000502882) nc_transcript_variant(ENST00000502882) upstream_gene_variant(ENST00000323865; ENST00000506598)
No. of Studies	1 (significant: 1; non-significant: 0; trend: 0)
Source	Literature-origin

SNP related studies (count: 1)

Reference	Allele Change	Risk Allele	Statistical Values	Author Comments	Result of Statistical Analysis
Shim SH, 2010	G/C		Multivariate model for genotype 'GG' P-value=0.834, OR=0.88;...... Multivariate model for genotype 'GG' P-value=0.834, OR=0.88; genotype 'CG' OR=1; genotype 'CC' P-value=0.039, OR=2.12; Multivariate model for allele, 'G' OR=1; allele 'C' P-value=0.026, OR=1.79 More...	statistically significant differences in the genotype distri...... statistically significant differences in the genotype distributions and allele frequencies and the homozygous allele C frequency was significantly higher in ADHD patients than in controls More...	Significant

SNP related genes (count: 1)

Literature-origin genes (count: 1)

Genes from other sources (count: 0)

SNPs in LD with rs6295 (count: 0) View in gBrowse (chr5:63258565..63258565 )