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	rs2327269 dbSNP Ensembl
Location	Chr20:10303128(Fwd)
Variant Alleles	T/C
Ancestral Allele	C
Functional Annotation	intron_variant; nc_transcript_variant.
Consequence to Transcript	intron_variant(ENST00000421143; ENST00000453544) nc_transcript_variant(ENST00000421143; ENST00000453544)
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	T/C	C	Single marker analysis FBAT P-value=0.013; Exploratory analy...... Single marker analysis FBAT P-value=0.013; Exploratory analyses FBAT P-value=0.248 for co-morbid CD, P-value=0.013 for co-morbid MDD, P-value=0.127 for co-morbid BD More...	Single marker and exploratory analysis showed evidence of si...... Single marker 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 rs2327269 (count: 0) View in gBrowse (chr20:10303128..10303128 )