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	rs362993 dbSNP Ensembl
Location	Chr20:10276716(Fwd)
Variant Alleles	C/T
Ancestral Allele	C
Functional Annotation	downstream_gene_variant; intron_variant; nc_transcript_variant; upstream_gene_variant.
Consequence to Transcript	downstream_gene_variant(ENST00000430336) intron_variant(ENST00000421143; ENST00000254976; ENST00000304886; ENST00000453544) nc_transcript_variant(ENST00000421143; ENST00000453544) upstream_gene_variant(ENST00000495883)
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
Kim JW, 2007	C/T	T	Single marker analysis FBAT P-value=1; Exploratory analyses ...... Single marker analysis FBAT P-value=1; Exploratory analyses FBAT P-value=0.275 for co-morbid CD, P-value=0.53 for co-morbid MDD, P-value=0.046 for co-morbid BD More...	Exploratory analysis showed evidence of significant associat...... Exploratory analysis showed evidence of significant association with ADHD and co-morbid BD More...	Significant

SNP related genes (count: 2)

Literature-origin genes (count: 1)

Genes from other sources (count: 1)

SNPs in LD with rs362993 (count: 0) View in gBrowse (chr20:10276716..10276716 )