rs796052578

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(C;C)	0	common in clinvar

Make rs796052578(-;-)

Make rs796052578(-;C)

Reference

GRCh38.p2 38.2/146

Chromosome

12

Position

13567034

Gene

GRIN2B

is a	snp
is	mentioned by
dbSNP	rs796052578
dbSNP (classic)	rs796052578
ClinGen	rs796052578
ebi	rs796052578
HLI	rs796052578
Exac	rs796052578
Gnomad	rs796052578
Varsome	rs796052578
LitVar	rs796052578
Map	rs796052578
PheGenI	rs796052578
Biobank	rs796052578
1000 genomes	rs796052578
hgdp	rs796052578
ensembl	rs796052578
geneview	rs796052578
scholar	rs796052578
google	rs796052578
pharmgkb	rs796052578
gwascentral	rs796052578
openSNP	rs796052578
23andMe	rs796052578
SNPshot	rs796052578
SNPdbe	rs796052578
MSV3d	rs796052578
GWAS Ctlg	rs796052578

Max Magnitude

0

ClinVar
Risk	rs796052578(-;-)
Alt	rs796052578(-;-)
Reference	Rs796052578(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	GRIN2B
CLNDBN	not provided
Reversed	1
HGVS	NC_000012.11:g.13719968delG
CLNSRC
CLNACC	RCV000187708.2,