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	rs6657749 dbSNP Ensembl
Location	Chr1:214576513(Fwd)
Variant Alleles	C/T
Ancestral Allele	T
Functional Annotation	intron_variant.
Consequence to Transcript	intron_variant(ENST00000366956; ENST00000543945)
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	T:C		Corrected TDT P-value=2.99E-05 (OR=0.6643) Corrected TDT P-value=2.99E-05 (OR=0.6643)	One of top 25 results in corrected TDT test One of top 25 results in corrected TDT test	Non-significant
Lantieri F, 2010	T:C		Binomial P-value=0.59, OR=1.03 for whole sample; Binomial P-...... Binomial P-value=0.59, OR=1.03 for whole sample; Binomial P-value=0.76, OR=1.13 for C-subtype More...	no significant association no significant association	Non-significant

SNP related genes (count: 1)

Literature-origin genes (count: 0)

Genes from other sources (count: 1)

SNPs in LD with rs6657749 (count: 0) View in gBrowse (chr1:214576513..214576513 )