rs1064796752

Orientation

minus

Stabilized

minus

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

Chromosome

12

Position

13569848

Gene

GRIN2B

is a	snp
is	mentioned by
dbSNP	rs1064796752
dbSNP (classic)	rs1064796752
ClinGen	rs1064796752
ebi	rs1064796752
HLI	rs1064796752
Exac	rs1064796752
Gnomad	rs1064796752
Varsome	rs1064796752
LitVar	rs1064796752
Map	rs1064796752
PheGenI	rs1064796752
Biobank	rs1064796752
1000 genomes	rs1064796752
hgdp	rs1064796752
ensembl	rs1064796752
geneview	rs1064796752
scholar	rs1064796752
google	rs1064796752
pharmgkb	rs1064796752
gwascentral	rs1064796752
openSNP	rs1064796752
23andMe	rs1064796752
SNPshot	rs1064796752
SNPdbe	rs1064796752
MSV3d	rs1064796752
GWAS Ctlg	rs1064796752

Max Magnitude

0

ClinVar
Risk	rs1064796752(G;G)
Alt	rs1064796752(G;G)
Reference	Rs1064796752(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	GRIN2B
CLNDBN	not provided
Reversed	1
HGVS	NC_000012.11:g.13722782G>C
CLNSRC
CLNACC	RCV000486259.1,