rs1057518988

Orientation

minus

Stabilized

minus

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

Make rs1057518988(A;G)

Make rs1057518988(G;G)

Reference

GRCh38.p7 38.3/150

Chromosome

12

Position

13571859

Gene

GRIN2B

is a	snp
is	mentioned by
dbSNP	rs1057518988
dbSNP (classic)	rs1057518988
ClinGen	rs1057518988
ebi	rs1057518988
HLI	rs1057518988
Exac	rs1057518988
Gnomad	rs1057518988
Varsome	rs1057518988
LitVar	rs1057518988
Map	rs1057518988
PheGenI	rs1057518988
Biobank	rs1057518988
1000 genomes	rs1057518988
hgdp	rs1057518988
ensembl	rs1057518988
geneview	rs1057518988
scholar	rs1057518988
google	rs1057518988
pharmgkb	rs1057518988
gwascentral	rs1057518988
openSNP	rs1057518988
23andMe	rs1057518988
SNPshot	rs1057518988
SNPdbe	rs1057518988
MSV3d	rs1057518988
GWAS Ctlg	rs1057518988

Max Magnitude

0

ClinVar
Risk	rs1057518988(G;G)
Alt	rs1057518988(G;G)
Reference	Rs1057518988(A;A)
Significance	Probable-Pathogenic
Disease	Ataxia Seizure Disorders intellectual deficiency
Variation	info
Gene	GRIN2B
CLNDBN	Ataxia Seizure Disorders intellectual deficiency
Reversed	1
HGVS	NC_000012.11:g.13724793T>C
CLNSRC
CLNACC	RCV000414945.1,