ADHDgene Database

SNP Report

Basic Info

Name	rs2070062 dbSNP Ensembl
Location	Chr4:56355598(Fwd)
Variant Alleles	A/C
Ancestral Allele	A
Functional Annotation	5_prime_UTR_variant; NMD_transcript_variant; nc_transcript_variant; non_coding_exon_variant.
Consequence to Transcript	5_prime_UTR_variant(ENST00000381322; ENST00000309964; ENST00000513440; ENST00000435527) NMD_transcript_variant(ENST00000435527) nc_transcript_variant(ENST00000513033; ENST00000509151; ENST00000506747; ENST00000506923) non_coding_exon_variant(ENST00000513033; ENST00000509151; ENST00000506747; ENST00000506923)
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 rs2070062 (count: 1) View in gBrowse (chr4:56301369..56355598 )

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[CEU]; 1.0[CHB]; 1.0[JPT]; 1.0[YRI]