rs796052549

Orientation

minus

Stabilized

minus

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

Make rs796052549(A;A)

Make rs796052549(A;G)

Reference

GRCh38.p2 38.2/146

Chromosome

16

Position

9798442

Gene	GRIN2A, LOC105371077

is a	snp
is	mentioned by
dbSNP	rs796052549
dbSNP (classic)	rs796052549
ClinGen	rs796052549
ebi	rs796052549
HLI	rs796052549
Exac	rs796052549
Gnomad	rs796052549
Varsome	rs796052549
LitVar	rs796052549
Map	rs796052549
PheGenI	rs796052549
Biobank	rs796052549
1000 genomes	rs796052549
hgdp	rs796052549
ensembl	rs796052549
geneview	rs796052549
scholar	rs796052549
google	rs796052549
pharmgkb	rs796052549
gwascentral	rs796052549
openSNP	rs796052549
23andMe	rs796052549
SNPshot	rs796052549
SNPdbe	rs796052549
MSV3d	rs796052549
GWAS Ctlg	rs796052549

Max Magnitude

0

ClinVar
Risk	rs796052549(A;A)
Alt	rs796052549(A;A)
Reference	Rs796052549(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	GRIN2A
CLNDBN	not provided
Reversed	1
HGVS	NC_000016.9:g.9892299C>T
CLNSRC	UniProtKB (protein)
CLNACC	RCV000187643.2,