rs876661055

Orientation

minus

Stabilized

minus

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

Make rs876661055(C;C)

Make rs876661055(C;T)

Reference

GRCh38.p2 38.2/147

Chromosome

12

Position

13569937

Gene

GRIN2B

is a	snp
is	mentioned by
dbSNP	rs876661055
dbSNP (classic)	rs876661055
ClinGen	rs876661055
ebi	rs876661055
HLI	rs876661055
Exac	rs876661055
Gnomad	rs876661055
Varsome	rs876661055
LitVar	rs876661055
Map	rs876661055
PheGenI	rs876661055
Biobank	rs876661055
1000 genomes	rs876661055
hgdp	rs876661055
ensembl	rs876661055
geneview	rs876661055
scholar	rs876661055
google	rs876661055
pharmgkb	rs876661055
gwascentral	rs876661055
openSNP	rs876661055
23andMe	rs876661055
SNPshot	rs876661055
SNPdbe	rs876661055
MSV3d	rs876661055
GWAS Ctlg	rs876661055

Max Magnitude

0

ClinVar
Risk	rs876661055(C;C)
Alt	rs876661055(C;C)
Reference	Rs876661055(T;T)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	GRIN2B
CLNDBN	not provided
Reversed	1
HGVS	NC_000012.11:g.13722871A>G
CLNSRC
CLNACC	RCV000217622.1,