ADHDgene Database

SNP Report

Basic Info

Name	rs11073960 dbSNP Ensembl
Location	Chr15:91483257(Fwd)
Variant Alleles	C/G
Ancestral Allele	G
Functional Annotation	downstream_gene_variant; intron_variant; nc_transcript_variant; upstream_gene_variant.
Consequence to Transcript	downstream_gene_variant(ENST00000495068; ENST00000556482; ENST00000497152; ENST00000461266) intron_variant(ENST00000553671; ENST00000557212; ENST00000486253; ENST00000553358; ENST00000394275; ENST00000418476) nc_transcript_variant(ENST00000553671; ENST00000557212; ENST00000486253; ENST00000553358) upstream_gene_variant(ENST00000556704; ENST00000448987; ENST00000438890)
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
UNC45A	unc-45 homolog A (C. elegans)	15q26.1

SNPs in LD with rs11073960 (count: 1) View in gBrowse (chr15:91450441..91483257 )

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]

rs2677744	NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant; non_coding_exon_variant; upstream_gene_variant	1(0/0/1)	0.836[CEU]