ADHDgene Database

SNP Report

Basic Info

Name	rs2284415 dbSNP Ensembl
Location	Chr12:13918091(Fwd)
Variant Alleles	A/G
Ancestral Allele	G
Functional Annotation	intron_variant.
Consequence to Transcript	intron_variant(ENST00000279593)
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)
GRIN2B	glutamate receptor, ionotropic, N-methyl D-aspartate 2B	12p12	1(1/0/0)

SNPs in LD with rs2284415 (count: 1) View in gBrowse (chr12:13918091..13919214 )

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]

rs2284416	intron_variant	1(0/1/0)	1.0[CEU]; 0.911[CHB]; 1.0[JPT]