rs864309560

Orientation

minus

Stabilized

minus

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

Make rs864309560(A;A)

Make rs864309560(A;C)

Reference

GRCh38.p2 38.2/146

Chromosome

12

Position

13567193

Gene

GRIN2B

is a	snp
is	mentioned by
dbSNP	rs864309560
dbSNP (classic)	rs864309560
ClinGen	rs864309560
ebi	rs864309560
HLI	rs864309560
Exac	rs864309560
Gnomad	rs864309560
Varsome	rs864309560
LitVar	rs864309560
Map	rs864309560
PheGenI	rs864309560
Biobank	rs864309560
1000 genomes	rs864309560
hgdp	rs864309560
ensembl	rs864309560
geneview	rs864309560
scholar	rs864309560
google	rs864309560
pharmgkb	rs864309560
gwascentral	rs864309560
openSNP	rs864309560
23andMe	rs864309560
SNPshot	rs864309560
SNPdbe	rs864309560
MSV3d	rs864309560
GWAS Ctlg	rs864309560

Max Magnitude

0

ClinVar
Risk	rs864309560(A;A)
Alt	rs864309560(A;A)
Reference	Rs864309560(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	GRIN2B
CLNDBN	not provided
Reversed	1
HGVS	NC_000012.11:g.13720127G>T
CLNSRC
CLNACC	RCV000203067.1,