ADHDgene Database

SNP Report

Basic Info

Name	rs4595309 dbSNP Ensembl
Location	ChrX:7180530(Fwd)
Variant Alleles	G/T
Ancestral Allele	G
Functional Annotation	intron_variant.
Consequence to Transcript	intron_variant(ENST00000217961)
No. of Studies	0 (significant: 0; non-significant: 0; trend: 0)
Source	LD-proxy

SNP related studies (count: 0)

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 rs4595309 (count: 5) View in gBrowse (chrX:7066051..7243304 )

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]

rs6639786	intron_variant	1(1/0/0)	0.908[ASW]; 1.0[CEU]; 1.0[CHB]; 1.0[CHD]; 1.0[GIH]; 1.0[JPT]; 1.0[MKK]; 1.0[TSI]; 1.0[YRI]
rs1473666	downstream_gene_variant; intron_variant; nc_transcript_variant	1(0/1/0)	1.0[CHD]; 0.862[GIH]
rs5934769	intron_variant	1(1/0/0)	1.0[ASW]; 1.0[CEU]; 1.0[CHB]; 1.0[CHD]; 1.0[GIH]; 1.0[JPT]; 1.0[LWK]; 1.0[MEX]; 0.974[MKK]; 1.0[TSI]; 1.0[YRI]
rs4403552	intron_variant	1(0/1/0)	0.932[CHB]; 0.821[CHD]; 0.93[JPT]
rs5934740	intron_variant	2(0/2/0)	1.0[CEU]; 1.0[CHB]; 1.0[CHD]; 1.0[GIH]; 1.0[JPT]; 0.937[MEX]; 1.0[TSI]