rs796052551

Orientation

minus

Stabilized

minus

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

Make rs796052551(A;G)

Make rs796052551(G;G)

Reference

GRCh38.p2 38.2/146

Chromosome

16

Position

9768997

Gene

GRIN2A

is a	snp
is	mentioned by
dbSNP	rs796052551
dbSNP (classic)	rs796052551
ClinGen	rs796052551
ebi	rs796052551
HLI	rs796052551
Exac	rs796052551
Gnomad	rs796052551
Varsome	rs796052551
LitVar	rs796052551
Map	rs796052551
PheGenI	rs796052551
Biobank	rs796052551
1000 genomes	rs796052551
hgdp	rs796052551
ensembl	rs796052551
geneview	rs796052551
scholar	rs796052551
google	rs796052551
pharmgkb	rs796052551
gwascentral	rs796052551
openSNP	rs796052551
23andMe	rs796052551
SNPshot	rs796052551
SNPdbe	rs796052551
MSV3d	rs796052551
GWAS Ctlg	rs796052551

Max Magnitude

0

ClinVar
Risk	rs796052551(G;G)
Alt	rs796052551(G;G)
Reference	Rs796052551(A;A)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	GRIN2A
CLNDBN	not provided
Reversed	1
HGVS	NC_000016.9:g.9862854T>C
CLNSRC	UniProtKB (protein)
CLNACC	RCV000187645.2,