rs796052556

Orientation

minus

Stabilized

minus

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

Make rs796052556(C;C)

Make rs796052556(C;G)

Reference

GRCh38.p2 38.2/146

Chromosome

16

Position

9764203

Gene

GRIN2A

is a	snp
is	mentioned by
dbSNP	rs796052556
dbSNP (classic)	rs796052556
ClinGen	rs796052556
ebi	rs796052556
HLI	rs796052556
Exac	rs796052556
Gnomad	rs796052556
Varsome	rs796052556
LitVar	rs796052556
Map	rs796052556
PheGenI	rs796052556
Biobank	rs796052556
1000 genomes	rs796052556
hgdp	rs796052556
ensembl	rs796052556
geneview	rs796052556
scholar	rs796052556
google	rs796052556
pharmgkb	rs796052556
gwascentral	rs796052556
openSNP	rs796052556
23andMe	rs796052556
SNPshot	rs796052556
SNPdbe	rs796052556
MSV3d	rs796052556
GWAS Ctlg	rs796052556

Max Magnitude

0

ClinVar
Risk	rs796052556(C;C)
Alt	rs796052556(C;C)
Reference	Rs796052556(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	GRIN2A
CLNDBN	not provided
Reversed	1
HGVS	NC_000016.9:g.9858060C>G
CLNSRC
CLNACC	RCV000187656.1,