rs1057518520

Orientation

minus

Stabilized

minus

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

Make rs1057518520(-;GCTC)

Make rs1057518520(GCTC;GCTC)

Reference

GRCh38.p7 38.3/150

Chromosome

12

Position

13564228

Gene

GRIN2B

is a	snp
is	mentioned by
dbSNP	rs1057518520
dbSNP (classic)	rs1057518520
ClinGen	rs1057518520
ebi	rs1057518520
HLI	rs1057518520
Exac	rs1057518520
Gnomad	rs1057518520
Varsome	rs1057518520
LitVar	rs1057518520
Map	rs1057518520
PheGenI	rs1057518520
Biobank	rs1057518520
1000 genomes	rs1057518520
hgdp	rs1057518520
ensembl	rs1057518520
geneview	rs1057518520
scholar	rs1057518520
google	rs1057518520
pharmgkb	rs1057518520
gwascentral	rs1057518520
openSNP	rs1057518520
23andMe	rs1057518520
SNPshot	rs1057518520
SNPdbe	rs1057518520
MSV3d	rs1057518520
GWAS Ctlg	rs1057518520

Max Magnitude

0

ClinVar
Risk	rs1057518520(GCTC;GCTC)
Alt	rs1057518520(GCTC;GCTC)
Reference	Rs1057518520(-;-)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	GRIN2B
CLNDBN	not provided
Reversed	1
HGVS	NC_000012.11:g.13717163_13717166dupGAGC
CLNSRC
CLNACC	RCV000413196.1,