ADHDgene Database

SNP Report

Basic Info

Name	rs11730626 dbSNP Ensembl
Location	Chr4:149354289(Fwd)
Variant Alleles	C/T
Ancestral Allele	T
Functional Annotation	intron_variant.
Consequence to Transcript	intron_variant(ENST00000344721; ENST00000511528; ENST00000512865; ENST00000342437; ENST00000358102; ENST00000355292)
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)
NR3C2	nuclear receptor subfamily 3, group C, member 2	4q31	1(0/1/0)

SNPs in LD with rs11730626 (count: 1) View in gBrowse (chr4:149354289..149357475 )

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]

rs5522	missense_variant	1(0/1/0)	1.0[CEU]; 1.0[CHB]; 1.0[JPT]; 1.0[YRI]