rs796052547

Orientation

minus

Stabilized

minus

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

Make rs796052547(A;G)

Make rs796052547(G;G)

Reference

GRCh38.p2 38.2/146

Chromosome

16

Position

9822382

Gene

GRIN2A

is a	snp
is	mentioned by
dbSNP	rs796052547
dbSNP (classic)	rs796052547
ClinGen	rs796052547
ebi	rs796052547
HLI	rs796052547
Exac	rs796052547
Gnomad	rs796052547
Varsome	rs796052547
LitVar	rs796052547
Map	rs796052547
PheGenI	rs796052547
Biobank	rs796052547
1000 genomes	rs796052547
hgdp	rs796052547
ensembl	rs796052547
geneview	rs796052547
scholar	rs796052547
google	rs796052547
pharmgkb	rs796052547
gwascentral	rs796052547
openSNP	rs796052547
23andMe	rs796052547
SNPshot	rs796052547
SNPdbe	rs796052547
MSV3d	rs796052547
GWAS Ctlg	rs796052547

Max Magnitude

0

ClinVar
Risk	rs796052547(G;G)
Alt	rs796052547(G;G)
Reference	Rs796052547(A;A)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	GRIN2A
CLNDBN	not provided
Reversed	1
HGVS	NC_000016.9:g.9916239T>C
CLNSRC
CLNACC	RCV000187640.2,