rs397518450

Orientation

minus

Stabilized

minus

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

Make rs397518450(C;G)

Make rs397518450(G;G)

Reference

GRCh38 38.1/141

Chromosome

16

Position

9834227

Gene

GRIN2A

is a	snp
is	mentioned by
dbSNP	rs397518450
dbSNP (classic)	rs397518450
ClinGen	rs397518450
ebi	rs397518450
HLI	rs397518450
Exac	rs397518450
Gnomad	rs397518450
Varsome	rs397518450
LitVar	rs397518450
Map	rs397518450
PheGenI	rs397518450
Biobank	rs397518450
1000 genomes	rs397518450
hgdp	rs397518450
ensembl	rs397518450
geneview	rs397518450
scholar	rs397518450
google	rs397518450
pharmgkb	rs397518450
gwascentral	rs397518450
openSNP	rs397518450
23andMe	rs397518450
SNPshot	rs397518450
SNPdbe	rs397518450
MSV3d	rs397518450
GWAS Ctlg	rs397518450

Max Magnitude

0

ClinVar
Risk	rs397518450(G;G)
Alt	rs397518450(G;G)
Reference	Rs397518450(C;C)
Significance	Pathogenic
Disease	Epilepsy
Variation	info
Gene	GRIN2A
CLNDBN	Epilepsy, focal, with speech disorder and with or without mental retardation
Reversed	1
HGVS	NC_000016.9:g.9928084G>C
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000032867.28,