ADHDgene Database

SNP Report

Basic Info

Name	rs5933863 dbSNP Ensembl
Location	ChrX:7270694(Fwd)
Variant Alleles	G/A
Ancestral Allele	G
Functional Annotation	3_prime_UTR_variant.
Consequence to Transcript	3_prime_UTR_variant(ENST00000217961)
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
Brookes KJ, 2008(b)			TDT P-value=0.28, OR=1.26 TDT P-value=0.28, OR=1.26	not significantly associated not significantly associated	Non-significant

SNP related genes (count: 1)

Approved Symbol	Approved Name	Location	No. of Studies (significant/non-significant/trend)
STS	steroid sulfatase (microsomal), isozyme S	Xp22.32	3(2/1/0)

SNPs in LD with rs5933863 (count: 3) View in gBrowse (chrX:7169546..7270694 )

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	#studies(significant/non-significant/trend)	r²[population]

rs5934770	intron_variant	1(1/0/0)	0.862[CEU]

rs_ID	Functional Annotation	r²[population]
rs5934917	intron_variant	0.922[CEU]
rs5934915	intron_variant	0.922[CEU]