rs796052570

Orientation

minus

Stabilized

minus

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

Make rs796052570(A;G)

Make rs796052570(G;G)

Reference

GRCh38.p2 38.2/146

Chromosome

12

Position

13753879

Gene

GRIN2B

is a	snp
is	mentioned by
dbSNP	rs796052570
dbSNP (classic)	rs796052570
ClinGen	rs796052570
ebi	rs796052570
HLI	rs796052570
Exac	rs796052570
Gnomad	rs796052570
Varsome	rs796052570
LitVar	rs796052570
Map	rs796052570
PheGenI	rs796052570
Biobank	rs796052570
1000 genomes	rs796052570
hgdp	rs796052570
ensembl	rs796052570
geneview	rs796052570
scholar	rs796052570
google	rs796052570
pharmgkb	rs796052570
gwascentral	rs796052570
openSNP	rs796052570
23andMe	rs796052570
SNPshot	rs796052570
SNPdbe	rs796052570
MSV3d	rs796052570
GWAS Ctlg	rs796052570

Max Magnitude

0

ClinVar
Risk	rs796052570(G;G)
Alt	rs796052570(G;G)
Reference	Rs796052570(A;A)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	GRIN2B
CLNDBN	not provided
Reversed	1
HGVS	NC_000012.11:g.13906813T>C
CLNSRC
CLNACC	RCV000187696.1,