ADHDgene Database

SNP Report

Basic Info

Name	rs2476391 dbSNP Ensembl
Location	Chr13:50618504(Fwd)
Variant Alleles	T/C
Ancestral Allele	T
Functional Annotation	downstream_gene_variant; intron_variant; nc_transcript_variant; non_coding_exon_variant.
Consequence to Transcript	downstream_gene_variant(ENST00000449579; ENST00000433070; ENST00000384985; ENST00000421758; ENST00000385271; ENST00000443587) intron_variant(ENST00000416253; ENST00000425586) nc_transcript_variant(ENST00000416253; ENST00000235290; ENST00000438752; ENST00000425586; ENST00000458725) non_coding_exon_variant(ENST00000235290; ENST00000438752; ENST00000458725)
No. of Studies	0 (significant: 0; non-significant: 0; trend: 0)
Source	LD-proxy

SNP related studies (count: 0)

SNP related genes (count: 3)

Approved Symbol	Approved Name	Location	No. of Studies (significant/non-significant/trend)
DLEU2	deleted in lymphocytic leukemia 2 (non-protein coding)	13q14	1(0/0/1)

Approved Symbol	Approved Name	Location
MIR15A	microRNA 15a	13q14.2
MIR16-1	microRNA 16-1	13q14.2

SNPs in LD with rs2476391 (count: 1) View in gBrowse (chr13:50618504..50725514 )

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]

rs790531	intron_variant; nc_transcript_variant	1(0/0/1)	0.825[CEU]; 1.0[CHB]; 1.0[JPT]