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	rs3787283 dbSNP Ensembl
Location	Chr20:10284418(Fwd)
Variant Alleles	A/G
Ancestral Allele	A
Functional Annotation	intron_variant; nc_transcript_variant.
Consequence to Transcript	intron_variant(ENST00000453544; ENST00000421143; ENST00000254976; ENST00000304886; ENST00000495883) nc_transcript_variant(ENST00000453544; ENST00000421143; ENST00000495883)
No. of Studies	2 (significant: 1; non-significant: 1; trend: 0)
Source	Literature-origin

SNP related studies (count: 2)

Reference	Allele Change	Risk Allele	Statistical Values	Author Comments	Result of Statistical Analysis
Brookes K, 2006	A/G		UNPHASED TDT P-value=0.468; WHAP TDT P-value=0.082 UNPHASED TDT P-value=0.468; WHAP TDT P-value=0.082	no significant association was observed no significant association was observed	Non-significant
Kim JW, 2007	A/G	G	Single marker analysis FBAT P-value=0.002; Exploratory analy...... Single marker analysis FBAT P-value=0.002; Exploratory analyses FBAT P-value=0.101 for co-morbid CD, P-value=0.012 for co-morbid MDD, P-value=0.085 for co-morbid BD More...	Combined and exploratory analysis showed evidence of signifi...... Combined and exploratory analysis showed evidence of significant association with ADHD and co-morbid MDD More...	Significant

SNP related genes (count: 2)

Literature-origin genes (count: 1)

Genes from other sources (count: 1)

SNPs in LD with rs3787283 (count: 0) View in gBrowse (chr20:10284418..10284418 )