ADHDgene Database

SNP Report

Basic Info

Name	rs174589 dbSNP Ensembl
Location	Chr11:61615803(Fwd)
Variant Alleles	C/G
Ancestral Allele	C
Functional Annotation	downstream_gene_variant; intron_variant; nc_transcript_variant.
Consequence to Transcript	downstream_gene_variant(ENST00000518606; ENST00000517312; ENST00000520145) intron_variant(ENST00000257261; ENST00000522056; ENST00000278840; ENST00000521571; ENST00000355484; ENST00000543584; ENST00000521849) nc_transcript_variant(ENST00000543584)
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)
FADS2	fatty acid desaturase 2	11q12.2	3(3/0/0)

SNPs in LD with rs174589 (count: 1) View in gBrowse (chr11:61615803..61627881 )

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]

rs174611	intron_variant; nc_transcript_variant; upstream_gene_variant	1(1/0/0)	1.0[YRI]