ADHDgene Database

SNP Report

Basic Info

Name	rs174568 dbSNP Ensembl
Location	Chr11:61593816(Fwd)
Variant Alleles	C/T
Ancestral Allele	C
Functional Annotation	3_prime_UTR_variant; intron_variant; synonymous_variant; upstream_gene_variant.
Consequence to Transcript	3_prime_UTR_variant(ENST00000517839) intron_variant(ENST00000257261; ENST00000522056; ENST00000448607; ENST00000421879) synonymous_variant(ENST00000574708; ENST00000522639) upstream_gene_variant(ENST00000278840; ENST00000518606; ENST00000521849; ENST00000517312)
No. of Studies	0 (significant: 0; non-significant: 0; trend: 0)
Source	LD-proxy

SNP related studies (count: 0)

SNP related genes (count: 2)

Approved Symbol	Approved Name	Location	No. of Studies (significant/non-significant/trend)
FADS2	fatty acid desaturase 2	11q12.2	3(3/0/0)
FADS1	fatty acid desaturase 1	11q12-q13.1	3(1/2/0)

SNPs in LD with rs174568 (count: 2) View in gBrowse (chr11:61569306..61593816 )

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]

rs174548	5_prime_UTR_variant; intron_variant; nc_transcript_variant	1(0/1/0)	0.808[CEU]; 1.0[CHB]; 0.908[CHD]; 1.0[GIH]; 1.0[JPT]
rs174545	3_prime_UTR_variant; downstream_gene_variant; intron_variant	1(0/1/0)	1.0[CEU]; 1.0[CHB]; 1.0[JPT]; 1.0[YRI]