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	rs4923463 dbSNP Ensembl
Location	Chr11:27672500(Fwd)
Variant Alleles	A/G
Ancestral Allele	A
Functional Annotation	downstream_gene_variant; intron_variant; nc_transcript_variant.
Consequence to Transcript	downstream_gene_variant(ENST00000525528; ENST00000395986; ENST00000439476; ENST00000533246; ENST00000584049; ENST00000525950; ENST00000530861; ENST00000395983; ENST00000438929; ENST00000395978; ENST00000418212; ENST00000530786; ENST00000533131; ENST00000532997; ENST00000395981; ENST00000314915; ENST00000356660; ENST00000420794; ENST00000395980) intron_variant(ENST00000499008; ENST00000499568; ENST00000500662; ENST00000532965; ENST00000502161; ENST00000530686; ENST00000530313; ENST00000501176) nc_transcript_variant(ENST00000499008; ENST00000499568; ENST00000500662; ENST00000502161; ENST00000530686; ENST00000532965; ENST00000530313; ENST00000501176)
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
Lanktree M, 2008	G:A		X²=3.31, P-value=0.069 in the family-based sample...... X²=3.31, P-value=0.069 in the family-based sample; X²=1.96, P-value=0.16, OR=1.43 in the case-control sample; X²=5.32, P-value=0.021, OR=1.56 in the combined samples More...	showed association in the combined samples showed association in the combined samples	Significant

SNP related genes (count: 2)

Literature-origin genes (count: 1)

Genes from other sources (count: 1)

SNPs in LD with rs4923463 (count: 0) View in gBrowse (chr11:27672500..27672500 )