rs879253931

Orientation

minus

Stabilized

minus

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

Make rs879253931(C;T)

Make rs879253931(T;T)

Reference

GRCh38.p7 38.3/149

Chromosome

12

Position

13567084

Gene

GRIN2B

is a	snp
is	mentioned by
dbSNP	rs879253931
dbSNP (classic)	rs879253931
ClinGen	rs879253931
ebi	rs879253931
HLI	rs879253931
Exac	rs879253931
Gnomad	rs879253931
Varsome	rs879253931
LitVar	rs879253931
Map	rs879253931
PheGenI	rs879253931
Biobank	rs879253931
1000 genomes	rs879253931
hgdp	rs879253931
ensembl	rs879253931
geneview	rs879253931
scholar	rs879253931
google	rs879253931
pharmgkb	rs879253931
gwascentral	rs879253931
openSNP	rs879253931
23andMe	rs879253931
SNPshot	rs879253931
SNPdbe	rs879253931
MSV3d	rs879253931
GWAS Ctlg	rs879253931

Max Magnitude

0

ClinVar
Risk	rs879253931(T;T)
Alt	rs879253931(T;T)
Reference	Rs879253931(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	GRIN2B
CLNDBN	not provided
Reversed	1
HGVS	NC_000012.11:g.13720018G>A
CLNSRC
CLNACC	RCV000235247.1,