rs1060499659

Orientation

minus

Stabilized

minus

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

Make rs1060499659(A;A)

Make rs1060499659(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

12

Position

13615170

Gene	GRIN2B, LOC105369668

is a	snp
is	mentioned by
dbSNP	rs1060499659
dbSNP (classic)	rs1060499659
ClinGen	rs1060499659
ebi	rs1060499659
HLI	rs1060499659
Exac	rs1060499659
Gnomad	rs1060499659
Varsome	rs1060499659
LitVar	rs1060499659
Map	rs1060499659
PheGenI	rs1060499659
Biobank	rs1060499659
1000 genomes	rs1060499659
hgdp	rs1060499659
ensembl	rs1060499659
geneview	rs1060499659
scholar	rs1060499659
google	rs1060499659
pharmgkb	rs1060499659
gwascentral	rs1060499659
openSNP	rs1060499659
23andMe	rs1060499659
SNPshot	rs1060499659
SNPdbe	rs1060499659
MSV3d	rs1060499659
GWAS Ctlg	rs1060499659

Max Magnitude

0

ClinVar
Risk	rs1060499659(A;A)
Alt	rs1060499659(A;A)
Reference	Rs1060499659(G;G)
Significance	Probable-Pathogenic
Disease	Epileptic encephalopathy
Variation	info
Gene	GRIN2B
CLNDBN	Epileptic encephalopathy, early infantile, 27
Reversed	1
HGVS	NC_000012.11:g.13768104C>T
CLNSRC
CLNACC	RCV000449489.1,