ADHDgene Database

SNP Report

Basic Info

Name	rs4320932 dbSNP Ensembl
Location	Chr11:2171601(Fwd)
Variant Alleles	T/C
Ancestral Allele	T
Functional Annotation	NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant; upstream_gene_variant.
Consequence to Transcript	NMD_transcript_variant(ENST00000356578) downstream_gene_variant(ENST00000381363; ENST00000445504; ENST00000381361) intron_variant(ENST00000481781; ENST00000356578; ENST00000381319; ENST00000397270; ENST00000476874) nc_transcript_variant(ENST00000476874; ENST00000481781) upstream_gene_variant(ENST00000300632; ENST00000337883)
No. of Studies	0 (significant: 0; non-significant: 0; trend: 0)
Source	LD-proxy

SNP related studies (count: 0)

SNP related genes (count: 4)

Approved Symbol	Approved Name	Location
IGF2-AS	IGF2 antisense RNA	11p15.5
IGF2AS	insulin-like growth factor 2 antisense	11p15.5
IGF2	insulin-like growth factor 2 (somatomedin A)	11p15.5
INS-IGF2	INS-IGF2 readthrough	11p15.5

SNPs in LD with rs4320932 (count: 1) View in gBrowse (chr11:2171601..2186335 )

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]

rs2070762	downstream_gene_variant; intron_variant; upstream_gene_variant	2(1/1/0)	0.855[CHD]