ADHDgene Database

SNP Report

Basic Info

Name	rs9928908 dbSNP Ensembl
Location	Chr16:9971066(Fwd)
Variant Alleles	C/T
Ancestral Allele	T
Functional Annotation	intron_variant; nc_transcript_variant.
Consequence to Transcript	intron_variant(ENST00000396573; ENST00000566683; ENST00000396575; ENST00000562109; ENST00000330684; ENST00000404927; ENST00000535259) nc_transcript_variant(ENST00000566683)
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)
GRIN2A	glutamate receptor, ionotropic, N-methyl D-aspartate 2A	16p13.2	3(1/2/0)

SNPs in LD with rs9928908 (count: 2) View in gBrowse (chr16:9937980..9971066 )

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]

rs12920919	intron_variant	1(0/1/0)	1.0[JPT]
rs727605	intron_variant; nc_transcript_variant	1(0/1/0)	0.888[JPT]