ADHDgene Database

SNP Report

Basic Info

Name	rs1048004 dbSNP Ensembl
Location	Chr4:56300209(Fwd)
Variant Alleles	C/A
Ancestral Allele	C
Functional Annotation	3_prime_UTR_variant; downstream_gene_variant; nc_transcript_variant; non_coding_exon_variant.
Consequence to Transcript	3_prime_UTR_variant(ENST00000309964) downstream_gene_variant(ENST00000513440; ENST00000381322) nc_transcript_variant(ENST00000511124) non_coding_exon_variant(ENST00000511124)
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)
CLOCK	clock homolog (mouse)	4q12	2(2/0/0)

SNPs in LD with rs1048004 (count: 1) View in gBrowse (chr4:56300209..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)	1.0[ASW]; 0.846[CHD]; 1.0[GIH]; 0.803[JPT]; 0.958[LWK]; 0.982[MKK]; 0.92[TSI]