ADHDgene Database

SNP Report

Basic Info

Name	rs1350666 dbSNP Ensembl
Location	Chr4:75224590(Fwd)
Variant Alleles	T/C
Ancestral Allele	T
No. of Studies	1 (significant: 0; non-significant: 0; trend: 1)
Source	Literature-origin

SNP related studies (count: 1)

Reference	Allele Change	Risk Allele	Statistical Values	Author Comments	Result of Statistical Analysis
Lasky-Su J, 2008			P-value=8.30E-06 under Additive model for FBAT-PC all sympto...... P-value=8.30E-06 under Additive model for FBAT-PC all symptoms More...	association finding with P-value association finding with P-value	Trend

SNP related genes (count: 1)

Approved Symbol	Approved Name	Location	No. of Studies (significant/non-significant/trend)
EREG	epiregulin	4q21.21	1(0/0/1)

SNPs in LD with rs1350666 (count: 8) View in gBrowse (chr4:75216896..75248685 )

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

rs_ID	Functional Annotation	r²[population]
rs1993665	intron_variant; nc_transcript_variant	0.816[CEU]; 0.806[TSI]
rs7684408		0.816[CEU]
rs7671661	intron_variant; nc_transcript_variant	0.816[CEU]
rs6446993	intron_variant; nc_transcript_variant	0.816[CEU]
rs1563826	intron_variant; nc_transcript_variant	0.816[CEU]
rs7673295		0.816[CEU]; 0.834[TSI]
rs2367709	downstream_gene_variant; intron_variant; nc_transcript_variant	0.804[CEU]; 0.811[CHB]
rs12512409	intron_variant; nc_transcript_variant	0.816[CEU]