rs869312868

Orientation

minus

Stabilized

minus

Make rs869312868(A;A)

Make rs869312868(A;G)

Reference

GRCh38.p2 38.2/147

Chromosome

12

Position

13571910

Gene

GRIN2B

is a	snp
is	mentioned by
dbSNP	rs869312868
dbSNP (classic)	rs869312868
ClinGen	rs869312868
ebi	rs869312868
HLI	rs869312868
Exac	rs869312868
Gnomad	rs869312868
Varsome	rs869312868
LitVar	rs869312868
Map	rs869312868
PheGenI	rs869312868
Biobank	rs869312868
1000 genomes	rs869312868
hgdp	rs869312868
ensembl	rs869312868
geneview	rs869312868
scholar	rs869312868
google	rs869312868
pharmgkb	rs869312868
gwascentral	rs869312868
openSNP	rs869312868
23andMe	rs869312868
SNPshot	rs869312868
SNPdbe	rs869312868
MSV3d	rs869312868
GWAS Ctlg	rs869312868

Max Magnitude

0

ClinVar
Risk	rs869312868(A;A)
Alt	rs869312868(A;A)
Reference	Rs869312868(G;G)
Significance	Pathogenic
Disease	Mental retardation not provided
Variation	info
Gene	GRIN2B
CLNDBN	Mental retardation, autosomal dominant 6 not provided
Reversed	1
HGVS	NC_000012.11:g.13724844C>T
CLNSRC
CLNACC	RCV000210391.1, RCV000478281.1,