rs796052572

Orientation

minus

Stabilized

minus

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

Make rs796052572(C;T)

Make rs796052572(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

12

Position

13571915

Gene

GRIN2B

is a	snp
is	mentioned by
dbSNP	rs796052572
dbSNP (classic)	rs796052572
ClinGen	rs796052572
ebi	rs796052572
HLI	rs796052572
Exac	rs796052572
Gnomad	rs796052572
Varsome	rs796052572
LitVar	rs796052572
Map	rs796052572
PheGenI	rs796052572
Biobank	rs796052572
1000 genomes	rs796052572
hgdp	rs796052572
ensembl	rs796052572
geneview	rs796052572
scholar	rs796052572
google	rs796052572
pharmgkb	rs796052572
gwascentral	rs796052572
openSNP	rs796052572
23andMe	rs796052572
SNPshot	rs796052572
SNPdbe	rs796052572
MSV3d	rs796052572
GWAS Ctlg	rs796052572

Max Magnitude

0

ClinVar
Risk	rs796052572(T;T)
Alt	rs796052572(T;T)
Reference	Rs796052572(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	GRIN2B
CLNDBN	not provided
Reversed	1
HGVS	NC_000012.11:g.13724849G>A
CLNSRC
CLNACC	RCV000187698.1,