rs387906637

Orientation

minus

Stabilized

minus

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

Make rs387906637(C;T)

Make rs387906637(T;T)

Reference

GRCh38 38.1/141

Chromosome

16

Position

9938314

Gene

GRIN2A

is a	snp
is	mentioned by
dbSNP	rs387906637
dbSNP (classic)	rs387906637
ClinGen	rs387906637
ebi	rs387906637
HLI	rs387906637
Exac	rs387906637
Gnomad	rs387906637
Varsome	rs387906637
LitVar	rs387906637
Map	rs387906637
PheGenI	rs387906637
Biobank	rs387906637
1000 genomes	rs387906637
hgdp	rs387906637
ensembl	rs387906637
geneview	rs387906637
scholar	rs387906637
google	rs387906637
pharmgkb	rs387906637
gwascentral	rs387906637
openSNP	rs387906637
23andMe	rs387906637
SNPshot	rs387906637
SNPdbe	rs387906637
MSV3d	rs387906637
GWAS Ctlg	rs387906637

Max Magnitude

0

ClinVar
Risk	rs387906637(T;T)
Alt	rs387906637(T;T)
Reference	Rs387906637(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.10032171G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000022584.24,