rs796052562

Orientation

minus

Stabilized

minus

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

Make rs796052562(A;A)

Make rs796052562(A;C)

Reference

GRCh38.p2 38.2/146

Chromosome

16

Position

9829506

Gene

GRIN2A

is a	snp
is	mentioned by
dbSNP	rs796052562
dbSNP (classic)	rs796052562
ClinGen	rs796052562
ebi	rs796052562
HLI	rs796052562
Exac	rs796052562
Gnomad	rs796052562
Varsome	rs796052562
LitVar	rs796052562
Map	rs796052562
PheGenI	rs796052562
Biobank	rs796052562
1000 genomes	rs796052562
hgdp	rs796052562
ensembl	rs796052562
geneview	rs796052562
scholar	rs796052562
google	rs796052562
pharmgkb	rs796052562
gwascentral	rs796052562
openSNP	rs796052562
23andMe	rs796052562
SNPshot	rs796052562
SNPdbe	rs796052562
MSV3d	rs796052562
GWAS Ctlg	rs796052562

Max Magnitude

0

ClinVar
Risk	rs796052562(A;A)
Alt	rs796052562(A;A)
Reference	Rs796052562(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	GRIN2A
CLNDBN	not provided
Reversed	1
HGVS	NC_000016.9:g.9923363G>T
CLNSRC
CLNACC	RCV000187675.1,