rs1057523843

Orientation

minus

Stabilized

minus

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

Make rs1057523843(C;C)

Make rs1057523843(C;G)

Reference

GRCh38.p7 38.3/150

Chromosome

16

Position

9840656

Gene

GRIN2A

is a	snp
is	mentioned by
dbSNP	rs1057523843
dbSNP (classic)	rs1057523843
ClinGen	rs1057523843
ebi	rs1057523843
HLI	rs1057523843
Exac	rs1057523843
Gnomad	rs1057523843
Varsome	rs1057523843
LitVar	rs1057523843
Map	rs1057523843
PheGenI	rs1057523843
Biobank	rs1057523843
1000 genomes	rs1057523843
hgdp	rs1057523843
ensembl	rs1057523843
geneview	rs1057523843
scholar	rs1057523843
google	rs1057523843
pharmgkb	rs1057523843
gwascentral	rs1057523843
openSNP	rs1057523843
23andMe	rs1057523843
SNPshot	rs1057523843
SNPdbe	rs1057523843
MSV3d	rs1057523843
GWAS Ctlg	rs1057523843

Max Magnitude

0

ClinVar
Risk	rs1057523843(C;C)
Alt	rs1057523843(C;C)
Reference	Rs1057523843(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	GRIN2A
CLNDBN	not provided
Reversed	1
HGVS	NC_000016.9:g.9934513C>G
CLNSRC
CLNACC	RCV000441942.1,