rs869312681

Orientation

minus

Stabilized

minus

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

Make rs869312681(A;G)

Make rs869312681(G;G)

Reference

GRCh38.p2 38.2/147

Chromosome

16

Position

9763169

Gene

GRIN2A

is a	snp
is	mentioned by
dbSNP	rs869312681
dbSNP (classic)	rs869312681
ClinGen	rs869312681
ebi	rs869312681
HLI	rs869312681
Exac	rs869312681
Gnomad	rs869312681
Varsome	rs869312681
LitVar	rs869312681
Map	rs869312681
PheGenI	rs869312681
Biobank	rs869312681
1000 genomes	rs869312681
hgdp	rs869312681
ensembl	rs869312681
geneview	rs869312681
scholar	rs869312681
google	rs869312681
pharmgkb	rs869312681
gwascentral	rs869312681
openSNP	rs869312681
23andMe	rs869312681
SNPshot	rs869312681
SNPdbe	rs869312681
MSV3d	rs869312681
GWAS Ctlg	rs869312681

Max Magnitude

0

ClinVar
Risk	rs869312681(G;G)
Alt	rs869312681(G;G)
Reference	Rs869312681(A;A)
Significance	Probable-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.9857026T>C
CLNSRC
CLNACC	RCV000209878.1,