rs796052550

Orientation

minus

Stabilized

minus

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

Make rs796052550(A;A)

Make rs796052550(A;G)

Reference

GRCh38.p2 38.2/146

Chromosome

16

Position

9798436

Gene	GRIN2A, LOC105371077

is a	snp
is	mentioned by
dbSNP	rs796052550
dbSNP (classic)	rs796052550
ClinGen	rs796052550
ebi	rs796052550
HLI	rs796052550
Exac	rs796052550
Gnomad	rs796052550
Varsome	rs796052550
LitVar	rs796052550
Map	rs796052550
PheGenI	rs796052550
Biobank	rs796052550
1000 genomes	rs796052550
hgdp	rs796052550
ensembl	rs796052550
geneview	rs796052550
scholar	rs796052550
google	rs796052550
pharmgkb	rs796052550
gwascentral	rs796052550
openSNP	rs796052550
23andMe	rs796052550
SNPshot	rs796052550
SNPdbe	rs796052550
MSV3d	rs796052550
GWAS Ctlg	rs796052550

Max Magnitude

0

ClinVar
Risk	rs796052550(A;A)
Alt	rs796052550(A;A)
Reference	Rs796052550(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	GRIN2A
CLNDBN	not provided
Reversed	1
HGVS	NC_000016.9:g.9892293C>T
CLNSRC
CLNACC	RCV000187644.2,