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	rs4913069 dbSNP Ensembl
Location	Chr5:139545110(Fwd)
Variant Alleles	G/A
Ancestral Allele	G
Functional Annotation	intron_variant; nc_transcript_variant.
Consequence to Transcript	intron_variant(ENST00000523154) nc_transcript_variant(ENST00000523154)
No. of Studies	2 (significant: 0; non-significant: 2; trend: 0)
Source	Literature-origin

SNP related studies (count: 2)

Reference	Allele Change	Risk Allele	Statistical Values	Author Comments	Result of Statistical Analysis
Neale BM, 2008	A:G		Uncorrected TDT P-value=6.94E-05 (OR=0.6476) Uncorrected TDT P-value=6.94E-05 (OR=0.6476)	One of top 25 results in uncorrected TDT test One of top 25 results in uncorrected TDT test	Non-significant
Lantieri F, 2010	A:G		Binomial P-value=0.5, OR=0.99 for whole sample; Binomial P-v...... Binomial P-value=0.5, OR=0.99 for whole sample; Binomial P-value=0.69, OR=1.08 for C-subtype More...	no significant association no significant association	Non-significant

SNP related genes (count: 0)

SNPs in LD with rs4913069 (count: 0) View in gBrowse (chr5:139545110..139545110 )