ADHDgene Database

SNP Report

Basic Info

Name	rs325456 dbSNP Ensembl
Location	Chr7:34843811(Fwd)
Variant Alleles	T/C
Ancestral Allele	C
Functional Annotation	NMD_transcript_variant; intron_variant; nc_transcript_variant.
Consequence to Transcript	NMD_transcript_variant(ENST00000396095; ENST00000381544) intron_variant(ENST00000436945; ENST00000539747; ENST00000431669; ENST00000360581; ENST00000396095; ENST00000442669; ENST00000535640; ENST00000359791; ENST00000381542; ENST00000381544; ENST00000531252; ENST00000381539) nc_transcript_variant(ENST00000436945; ENST00000539747; ENST00000431669; ENST00000442669; ENST00000535640)
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	No. of Studies (significant/non-significant/trend)
NPSR1	neuropeptide S receptor 1	7p14.3	1(0/1/0)

Approved Symbol	Approved Name	Location
NPSR1-AS1	NPSR1 antisense RNA 1	7p14.3

SNPs in LD with rs325456 (count: 1) View in gBrowse (chr7:34818113..34843811 )

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]

rs324981	NMD_transcript_variant; intron_variant; missense_variant; nc_transcript_variant	1(0/1/0)	0.866[CHB]; 0.976[CHD]; 0.953[JPT]