ADHDgene Database

SNP Report

Basic Info

Name	rs151976 dbSNP Ensembl
Location	Chr5:112236448(Fwd)
Variant Alleles	C/T
Ancestral Allele	C
Functional Annotation	NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant.
Consequence to Transcript	NMD_transcript_variant(ENST00000511865) downstream_gene_variant(ENST00000579867) intron_variant(ENST00000474542; ENST00000261482; ENST00000511865; ENST00000379638; ENST00000497856; ENST00000545426; ENST00000504247; ENST00000513339) nc_transcript_variant(ENST00000474542; ENST00000497856)
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)
REEP5	receptor accessory protein 5	5q22-q23	1(0/0/1)

SNPs in LD with rs151976 (count: 1) View in gBrowse (chr5:112236448..112242968 )

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]

rs469727	NMD_transcript_variant; intron_variant; nc_transcript_variant; upstream_gene_variant	1(0/0/1)	0.87[CEU]