rs201439880

Orientation

plus

Stabilized

plus

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

Make rs201439880(A;A)

Make rs201439880(A;G)

Reference

GRCh38.p7 38.3/149

Chromosome

12

Position

13564226

Gene

GRIN2B

is a	snp
is	mentioned by
dbSNP	rs201439880
dbSNP (classic)	rs201439880
ClinGen	rs201439880
ebi	rs201439880
HLI	rs201439880
Exac	rs201439880
Gnomad	rs201439880
Varsome	rs201439880
LitVar	rs201439880
Map	rs201439880
PheGenI	rs201439880
Biobank	rs201439880
1000 genomes	rs201439880
hgdp	rs201439880
ensembl	rs201439880
geneview	rs201439880
scholar	rs201439880
google	rs201439880
pharmgkb	rs201439880
gwascentral	rs201439880
openSNP	rs201439880
23andMe	rs201439880
SNPshot	rs201439880
SNPdbe	rs201439880
MSV3d	rs201439880
GWAS Ctlg	rs201439880

Max Magnitude

0

ClinVar
Risk	rs201439880(A;A) rs201439880(C;C)
Alt	rs201439880(A;A) rs201439880(C;C)
Reference	Rs201439880(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	GRIN2B
CLNDBN	not provided
Reversed	0
HGVS	NC_000012.11:g.13717160G>C
CLNSRC
CLNACC	RCV000353647.1,