rs886042168

Orientation

plus

Stabilized

plus

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

Chromosome

16

Position

9764654

Gene

GRIN2A

is a	snp
is	mentioned by
dbSNP	rs886042168
dbSNP (classic)	rs886042168
ClinGen	rs886042168
ebi	rs886042168
HLI	rs886042168
Exac	rs886042168
Gnomad	rs886042168
Varsome	rs886042168
LitVar	rs886042168
Map	rs886042168
PheGenI	rs886042168
Biobank	rs886042168
1000 genomes	rs886042168
hgdp	rs886042168
ensembl	rs886042168
geneview	rs886042168
scholar	rs886042168
google	rs886042168
pharmgkb	rs886042168
gwascentral	rs886042168
openSNP	rs886042168
23andMe	rs886042168
SNPshot	rs886042168
SNPdbe	rs886042168
MSV3d	rs886042168
GWAS Ctlg	rs886042168

Max Magnitude

0

ClinVar
Risk	rs886042168(-;-)
Alt	rs886042168(-;-)
Reference	Rs886042168(G;G)
Significance	Pathogenic
Disease	Epilepsy
Variation	info
Gene	GRIN2A
CLNDBN	Epilepsy, focal, with speech disorder and with or without mental retardation
Reversed	0
HGVS	NC_000016.9:g.9858511delG
CLNSRC
CLNACC	RCV000328046.1,