ADHDgene Database

SNP Report

Basic Info

Name	rs10823952 dbSNP Ensembl
Location	Chr10:53771139(Fwd)
Variant Alleles	G/A
Ancestral Allele	G
Functional Annotation	intron_variant.
Consequence to Transcript	intron_variant(ENST00000373985; ENST00000373980; ENST00000373976; ENST00000401604)
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)
PRKG1	protein kinase, cGMP-dependent, type I	10q11.2	1(0/0/1)

SNPs in LD with rs10823952 (count: 5) View in gBrowse (chr10:53771139..53787957 )

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]

rs10823954	intron_variant	1(0/1/0)	0.942[CHB]; 0.844[JPT]
rs7893146	intron_variant	1(0/1/0)	0.942[CHB]; 0.844[JPT]
rs1903979	intron_variant	1(0/1/0)	0.942[CHB]; 0.844[JPT]
rs1903977	intron_variant	1(0/0/1)	0.942[CHB]; 0.844[JPT]
rs10823978	intron_variant	1(0/1/0)	0.942[CHB]