ADHDgene Database

SNP Report

Basic Info

Name	rs11732723 dbSNP Ensembl
Location	Chr4:56290558(Fwd)
Variant Alleles	C/T
Ancestral Allele	T
Functional Annotation	NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant; non_coding_exon_variant.
Consequence to Transcript	NMD_transcript_variant(ENST00000508404) downstream_gene_variant(ENST00000309964) intron_variant(ENST00000542052; ENST00000381334; ENST00000514904; ENST00000508561; ENST00000508404; ENST00000509575; ENST00000506103; ENST00000506198) nc_transcript_variant(ENST00000515591; ENST00000514904; ENST00000508561; ENST00000509575; ENST00000506103) non_coding_exon_variant(ENST00000515591)
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)
CLOCK	clock homolog (mouse)	4q12	2(2/0/0)

Approved Symbol	Approved Name	Location
TMEM165	transmembrane protein 165	4q12

SNPs in LD with rs11732723 (count: 1) View in gBrowse (chr4:56290558..56301369 )

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]

rs1801260	3_prime_UTR_variant; nc_transcript_variant; non_coding_exon_variant	2(2/0/0)	0.814[GIH]; 1.0[JPT]