rs796052563

Orientation

minus

Stabilized

minus

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

Make rs796052563(A;A)

Make rs796052563(A;G)

Reference

GRCh38.p2 38.2/146

Chromosome

16

Position

9822348

Gene

GRIN2A

is a	snp
is	mentioned by
dbSNP	rs796052563
dbSNP (classic)	rs796052563
ClinGen	rs796052563
ebi	rs796052563
HLI	rs796052563
Exac	rs796052563
Gnomad	rs796052563
Varsome	rs796052563
LitVar	rs796052563
Map	rs796052563
PheGenI	rs796052563
Biobank	rs796052563
1000 genomes	rs796052563
hgdp	rs796052563
ensembl	rs796052563
geneview	rs796052563
scholar	rs796052563
google	rs796052563
pharmgkb	rs796052563
gwascentral	rs796052563
openSNP	rs796052563
23andMe	rs796052563
SNPshot	rs796052563
SNPdbe	rs796052563
MSV3d	rs796052563
GWAS Ctlg	rs796052563

Max Magnitude

0

ClinVar
Risk	rs796052563(A;A)
Alt	rs796052563(A;A)
Reference	Rs796052563(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	GRIN2A
CLNDBN	not provided
Reversed	1
HGVS	NC_000016.9:g.9916205C>T
CLNSRC
CLNACC	RCV000187676.1,