ADHDgene Database

SNP Report

Basic Info

Name	rs689687 dbSNP Ensembl
Location	Chr9:93410201(Fwd)
Variant Alleles	T/C
Ancestral Allele	T
Functional Annotation	upstream_gene_variant.
Consequence to Transcript	upstream_gene_variant(ENST00000375765)
No. of Studies	1 (significant: 0; non-significant: 1; trend: 0)
Source	Literature-origin

SNP related studies (count: 1)

Reference	Allele Change	Risk Allele	Statistical Values	Author Comments	Result of Statistical Analysis
Reif, A., 2011	T/C		P-value=0.6039, OR (allele)=1.07 (C), 95% CI=0.84-1.36 in Ge...... P-value=0.6039, OR (allele)=1.07 (C), 95% CI=0.84-1.36 in German discovery sample; P-value=0.3791, OR (allele)=1.07 (T), 95% CI=0.92-1.24 in IMpACT replication sample; P-value=0.6344, OR (allele)=1.03 (T), 95% CI=0.91-1.17 in pooled data; PDT P-value=0.1456 for allele T in the family-based analysis More...	This SNP did not reach p<0.05 in the association test with a...... This SNP did not reach p<0.05 in the association test with aADHD. Replication in 1035 aADHD patients and 1381 controls from IMpACT did not show any significant SNP association. More...	Non-significant

SNP related genes (count: 1)

Approved Symbol	Approved Name	Location	No. of Studies (significant/non-significant/trend)
DIRAS2	DIRAS family, GTP-binding RAS-like 2	9q22.32	1(1/0/0)

SNPs in LD with rs689687 (count: 5) View in gBrowse (chr9:93377223..93433370 )

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