rs397518472

Orientation

minus

Stabilized

minus

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

Make rs397518472(C;T)

Make rs397518472(T;T)

Reference

GRCh38 38.1/141

Chromosome

16

Position

9822391

Gene

GRIN2A

is a	snp
is	mentioned by
dbSNP	rs397518472
dbSNP (classic)	rs397518472
ClinGen	rs397518472
ebi	rs397518472
HLI	rs397518472
Exac	rs397518472
Gnomad	rs397518472
Varsome	rs397518472
LitVar	rs397518472
Map	rs397518472
PheGenI	rs397518472
Biobank	rs397518472
1000 genomes	rs397518472
hgdp	rs397518472
ensembl	rs397518472
geneview	rs397518472
scholar	rs397518472
google	rs397518472
pharmgkb	rs397518472
gwascentral	rs397518472
openSNP	rs397518472
23andMe	rs397518472
SNPshot	rs397518472
SNPdbe	rs397518472
MSV3d	rs397518472
GWAS Ctlg	rs397518472

Max Magnitude

0

ClinVar
Risk	rs397518472(T;T)
Alt	rs397518472(T;T)
Reference	Rs397518472(C;C)
Significance	Pathogenic
Disease	Epilepsy not provided
Variation	info
Gene	GRIN2A
CLNDBN	Epilepsy, focal, with speech disorder and with or without mental retardation not provided
Reversed	1
HGVS	NC_000016.9:g.9916248G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000074393.26, RCV000260469.1,