ADHDgene Database

SNP Report

Basic Info

Name	rs871078 dbSNP Ensembl
Location	Chr15:91478050(Fwd)
Variant Alleles	G/T
Ancestral Allele	T
Functional Annotation	downstream_gene_variant; intron_variant; nc_transcript_variant; upstream_gene_variant.
Consequence to Transcript	downstream_gene_variant(ENST00000556319) intron_variant(ENST00000480470; ENST00000394275; ENST00000461266; ENST00000553358; ENST00000448987; ENST00000438890) nc_transcript_variant(ENST00000480470; ENST00000461266; ENST00000553358; ENST00000448987; ENST00000438890) upstream_gene_variant(ENST00000497152; ENST00000557212; ENST00000553671; ENST00000556482; ENST00000495068; ENST00000418476; ENST00000486253; ENST00000394272; ENST00000561036; ENST00000559834; ENST00000330334; ENST00000494993; ENST00000559898)
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
UNC45A	unc-45 homolog A (C. elegans)	15q26.1
HDDC3	HD domain containing 3	15q26.1

SNPs in LD with rs871078 (count: 1) View in gBrowse (chr15:91450441..91478050 )

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)	1.0[CEU]; 0.806[TSI]