rs876661076

Orientation

minus

Stabilized

minus

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

Make rs876661076(A;C)

Make rs876661076(C;C)

Reference

GRCh38.p2 38.2/147

Chromosome

12

Position

13567171

Gene

GRIN2B

is a	snp
is	mentioned by
dbSNP	rs876661076
dbSNP (classic)	rs876661076
ClinGen	rs876661076
ebi	rs876661076
HLI	rs876661076
Exac	rs876661076
Gnomad	rs876661076
Varsome	rs876661076
LitVar	rs876661076
Map	rs876661076
PheGenI	rs876661076
Biobank	rs876661076
1000 genomes	rs876661076
hgdp	rs876661076
ensembl	rs876661076
geneview	rs876661076
scholar	rs876661076
google	rs876661076
pharmgkb	rs876661076
gwascentral	rs876661076
openSNP	rs876661076
23andMe	rs876661076
SNPshot	rs876661076
SNPdbe	rs876661076
MSV3d	rs876661076
GWAS Ctlg	rs876661076

Max Magnitude

0

ClinVar
Risk	rs876661076(C;C)
Alt	rs876661076(C;C)
Reference	Rs876661076(A;A)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	GRIN2B
CLNDBN	not provided
Reversed	1
HGVS	NC_000012.11:g.13720105T>G
CLNSRC
CLNACC	RCV000214028.1,