ADHDgene Database

SNP Report

Basic Info

Name	rs9809240 dbSNP Ensembl
Location	Chr3:33665652(Fwd)
Variant Alleles	T/C
Ancestral Allele	C
Functional Annotation	downstream_gene_variant; intron_variant; nc_transcript_variant.
Consequence to Transcript	downstream_gene_variant(ENST00000498331) intron_variant(ENST00000496954; ENST00000313350; ENST00000399362; ENST00000482896; ENST00000485378; ENST00000461133; ENST00000487200; ENST00000468888; ENST00000333778; ENST00000480013; ENST00000476433; ENST00000359576; ENST00000307312; ENST00000539981) nc_transcript_variant(ENST00000482896; ENST00000476433)
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)
CLASP2	cytoplasmic linker associated protein 2	3p24.3	1(0/0/1)

SNPs in LD with rs9809240 (count: 1) View in gBrowse (chr3:33665652..33774574 )

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]

rs9844608		1(0/0/1)	0.859[CHB]; 0.811[CHD]; 0.973[GIH]; 0.952[JPT]; 0.831[MEX]; 0.927[YRI]