rs869312916

Orientation

minus

Stabilized

minus

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

Make rs869312916(A;G)

Make rs869312916(G;G)

Reference

GRCh38.p2 38.2/147

Chromosome

16

Position

9829589

Gene

GRIN2A

is a	snp
is	mentioned by
dbSNP	rs869312916
dbSNP (classic)	rs869312916
ClinGen	rs869312916
ebi	rs869312916
HLI	rs869312916
Exac	rs869312916
Gnomad	rs869312916
Varsome	rs869312916
LitVar	rs869312916
Map	rs869312916
PheGenI	rs869312916
Biobank	rs869312916
1000 genomes	rs869312916
hgdp	rs869312916
ensembl	rs869312916
geneview	rs869312916
scholar	rs869312916
google	rs869312916
pharmgkb	rs869312916
gwascentral	rs869312916
openSNP	rs869312916
23andMe	rs869312916
SNPshot	rs869312916
SNPdbe	rs869312916
MSV3d	rs869312916
GWAS Ctlg	rs869312916

Max Magnitude

0

ClinVar
Risk	rs869312916(G;G)
Alt	rs869312916(G;G)
Reference	Rs869312916(A;A)
Significance	Pathogenic
Disease	Inborn genetic diseases
Variation	info
Gene	GRIN2A
CLNDBN	Inborn genetic diseases
Reversed	1
HGVS	NC_000016.9:g.9923446T>C
CLNSRC
CLNACC	RCV000210655.1,