rs1057524392

Orientation

minus

Stabilized

minus

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

Make rs1057524392(A;T)

Make rs1057524392(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

12

Position

13615621

Gene	GRIN2B, LOC105369668

is a	snp
is	mentioned by
dbSNP	rs1057524392
dbSNP (classic)	rs1057524392
ClinGen	rs1057524392
ebi	rs1057524392
HLI	rs1057524392
Exac	rs1057524392
Gnomad	rs1057524392
Varsome	rs1057524392
LitVar	rs1057524392
Map	rs1057524392
PheGenI	rs1057524392
Biobank	rs1057524392
1000 genomes	rs1057524392
hgdp	rs1057524392
ensembl	rs1057524392
geneview	rs1057524392
scholar	rs1057524392
google	rs1057524392
pharmgkb	rs1057524392
gwascentral	rs1057524392
openSNP	rs1057524392
23andMe	rs1057524392
SNPshot	rs1057524392
SNPdbe	rs1057524392
MSV3d	rs1057524392
GWAS Ctlg	rs1057524392

Max Magnitude

0

ClinVar
Risk	rs1057524392(T;T)
Alt	rs1057524392(T;T)
Reference	Rs1057524392(A;A)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	GRIN2B
CLNDBN	not provided
Reversed	1
HGVS	NC_000012.11:g.13768555T>A
CLNSRC
CLNACC	RCV000422130.1,