rs1057524089

Orientation

minus

Stabilized

minus

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

Make rs1057524089(C;T)

Make rs1057524089(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

16

Position

9938479

Gene

GRIN2A

is a	snp
is	mentioned by
dbSNP	rs1057524089
dbSNP (classic)	rs1057524089
ClinGen	rs1057524089
ebi	rs1057524089
HLI	rs1057524089
Exac	rs1057524089
Gnomad	rs1057524089
Varsome	rs1057524089
LitVar	rs1057524089
Map	rs1057524089
PheGenI	rs1057524089
Biobank	rs1057524089
1000 genomes	rs1057524089
hgdp	rs1057524089
ensembl	rs1057524089
geneview	rs1057524089
scholar	rs1057524089
google	rs1057524089
pharmgkb	rs1057524089
gwascentral	rs1057524089
openSNP	rs1057524089
23andMe	rs1057524089
SNPshot	rs1057524089
SNPdbe	rs1057524089
MSV3d	rs1057524089
GWAS Ctlg	rs1057524089

Max Magnitude

0

ClinVar
Risk	rs1057524089(T;T)
Alt	rs1057524089(T;T)
Reference	Rs1057524089(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	GRIN2A
CLNDBN	not provided
Reversed	1
HGVS	NC_000016.9:g.10032336G>A
CLNSRC
CLNACC	RCV000438586.1,