rs774592932

Orientation

plus

Stabilized

plus

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

Make rs774592932(A;A)

Make rs774592932(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

12

Position

13615213

Gene	GRIN2B, LOC105369668

is a	snp
is	mentioned by
dbSNP	rs774592932
dbSNP (classic)	rs774592932
ClinGen	rs774592932
ebi	rs774592932
HLI	rs774592932
Exac	rs774592932
Gnomad	rs774592932
Varsome	rs774592932
LitVar	rs774592932
Map	rs774592932
PheGenI	rs774592932
Biobank	rs774592932
1000 genomes	rs774592932
hgdp	rs774592932
ensembl	rs774592932
geneview	rs774592932
scholar	rs774592932
google	rs774592932
pharmgkb	rs774592932
gwascentral	rs774592932
openSNP	rs774592932
23andMe	rs774592932
SNPshot	rs774592932
SNPdbe	rs774592932
MSV3d	rs774592932
GWAS Ctlg	rs774592932

Max Magnitude

0

ClinVar
Risk	rs774592932(A;A)
Alt	rs774592932(A;A)
Reference	Rs774592932(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	GRIN2B
CLNDBN	not provided
Reversed	0
HGVS	NC_000012.11:g.13768147G>A
CLNSRC
CLNACC	RCV000426345.1,