rs797045015

Orientation

minus

Stabilized

minus

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

Make rs797045015(A;G)

Make rs797045015(G;G)

Reference

GRCh38.p2 38.2/146

Chromosome

16

Position

10180098

Gene

GRIN2A

is a	snp
is	mentioned by
dbSNP	rs797045015
dbSNP (classic)	rs797045015
ClinGen	rs797045015
ebi	rs797045015
HLI	rs797045015
Exac	rs797045015
Gnomad	rs797045015
Varsome	rs797045015
LitVar	rs797045015
Map	rs797045015
PheGenI	rs797045015
Biobank	rs797045015
1000 genomes	rs797045015
hgdp	rs797045015
ensembl	rs797045015
geneview	rs797045015
scholar	rs797045015
google	rs797045015
pharmgkb	rs797045015
gwascentral	rs797045015
openSNP	rs797045015
23andMe	rs797045015
SNPshot	rs797045015
SNPdbe	rs797045015
MSV3d	rs797045015
GWAS Ctlg	rs797045015

Max Magnitude

0

ClinVar
Risk	rs797045015(G;G)
Alt	rs797045015(G;G)
Reference	Rs797045015(A;A)
Significance	Probable-non-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.10273955T>C
CLNSRC
CLNACC	RCV000190515.2,