rs796052552

Orientation

minus

Stabilized

minus

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

Make rs796052552(C;T)

Make rs796052552(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

16

Position

9764696

Gene

GRIN2A

is a	snp
is	mentioned by
dbSNP	rs796052552
dbSNP (classic)	rs796052552
ClinGen	rs796052552
ebi	rs796052552
HLI	rs796052552
Exac	rs796052552
Gnomad	rs796052552
Varsome	rs796052552
LitVar	rs796052552
Map	rs796052552
PheGenI	rs796052552
Biobank	rs796052552
1000 genomes	rs796052552
hgdp	rs796052552
ensembl	rs796052552
geneview	rs796052552
scholar	rs796052552
google	rs796052552
pharmgkb	rs796052552
gwascentral	rs796052552
openSNP	rs796052552
23andMe	rs796052552
SNPshot	rs796052552
SNPdbe	rs796052552
MSV3d	rs796052552
GWAS Ctlg	rs796052552

Max Magnitude

0

ClinVar
Risk	rs796052552(T;T)
Alt	rs796052552(T;T)
Reference	Rs796052552(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	GRIN2A
CLNDBN	not provided
Reversed	1
HGVS	NC_000016.9:g.9858553G>A
CLNSRC
CLNACC	RCV000187646.1,