rs876661167

Orientation

minus

Stabilized

minus

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

Make rs876661167(A;A)

Make rs876661167(A;G)

Reference

GRCh38.p2 38.2/147

Chromosome

12

Position

13563906

Gene

GRIN2B

is a	snp
is	mentioned by
dbSNP	rs876661167
dbSNP (classic)	rs876661167
ClinGen	rs876661167
ebi	rs876661167
HLI	rs876661167
Exac	rs876661167
Gnomad	rs876661167
Varsome	rs876661167
LitVar	rs876661167
Map	rs876661167
PheGenI	rs876661167
Biobank	rs876661167
1000 genomes	rs876661167
hgdp	rs876661167
ensembl	rs876661167
geneview	rs876661167
scholar	rs876661167
google	rs876661167
pharmgkb	rs876661167
gwascentral	rs876661167
openSNP	rs876661167
23andMe	rs876661167
SNPshot	rs876661167
SNPdbe	rs876661167
MSV3d	rs876661167
GWAS Ctlg	rs876661167

Max Magnitude

0

ClinVar
Risk	rs876661167(A;A)
Alt	rs876661167(A;A)
Reference	Rs876661167(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	GRIN2B
CLNDBN	not provided
Reversed	1
HGVS	NC_000012.11:g.13716840C>T
CLNSRC
CLNACC	RCV000214952.2,