rs796052560

Orientation

minus

Stabilized

minus

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

Make rs796052560(-;-)

Make rs796052560(-;C)

Reference

GRCh38.p2 38.2/146

Chromosome

16

Position

9938339

Gene

GRIN2A

is a	snp
is	mentioned by
dbSNP	rs796052560
dbSNP (classic)	rs796052560
ClinGen	rs796052560
ebi	rs796052560
HLI	rs796052560
Exac	rs796052560
Gnomad	rs796052560
Varsome	rs796052560
LitVar	rs796052560
Map	rs796052560
PheGenI	rs796052560
Biobank	rs796052560
1000 genomes	rs796052560
hgdp	rs796052560
ensembl	rs796052560
geneview	rs796052560
scholar	rs796052560
google	rs796052560
pharmgkb	rs796052560
gwascentral	rs796052560
openSNP	rs796052560
23andMe	rs796052560
SNPshot	rs796052560
SNPdbe	rs796052560
MSV3d	rs796052560
GWAS Ctlg	rs796052560

Max Magnitude

0

ClinVar
Risk	rs796052560(-;-)
Alt	rs796052560(-;-)
Reference	Rs796052560(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	GRIN2A
CLNDBN	not provided
Reversed	1
HGVS	NC_000016.9:g.10032196delG
CLNSRC
CLNACC	RCV000187672.1,