ADHDgene Database

SNP Report

Basic Info

Name	rs4241112 dbSNP Ensembl
Location	Chr2:122662212(Fwd)
Variant Alleles	T/C
Ancestral Allele	C
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		Uncorrected TDT P-value=3.16E-05 (OR=0.7214); Corrected TDT ...... Uncorrected TDT P-value=3.16E-05 (OR=0.7214); Corrected TDT P-value=6.06E-05 (OR=0.7214) More...	One of top 25 results in both uncorrected and corrected TDT ...... One of top 25 results in both uncorrected and corrected TDT test More...	Non-significant
Lantieri F, 2010	T:C		Binomial P-value=0.11, OR=0.87 for whole sample; Binomial P-...... Binomial P-value=0.11, OR=0.87 for whole sample; Binomial P-value=0.91, OR=0.84 for C-subtype More...	no significant association no significant association	Non-significant

SNP related genes (count: 0)

SNPs in LD with rs4241112 (count: 4) View in gBrowse (chr2:122662212..122809849 )

The LD data used here is based on HapMap rel#27. LD SNP pairs were selected with a threshold r²>=0.8.