rs1057518577

Orientation

minus

Stabilized

minus

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

Make rs1057518577(GT;GT)

Make rs1057518577(GT;TA)

Reference

GRCh38.p7 38.3/150

Chromosome

12

Position

13611722

Gene	GRIN2B, LOC105369668

is a	snp
is	mentioned by
dbSNP	rs1057518577
dbSNP (classic)	rs1057518577
ClinGen	rs1057518577
ebi	rs1057518577
HLI	rs1057518577
Exac	rs1057518577
Gnomad	rs1057518577
Varsome	rs1057518577
LitVar	rs1057518577
Map	rs1057518577
PheGenI	rs1057518577
Biobank	rs1057518577
1000 genomes	rs1057518577
hgdp	rs1057518577
ensembl	rs1057518577
geneview	rs1057518577
scholar	rs1057518577
google	rs1057518577
pharmgkb	rs1057518577
gwascentral	rs1057518577
openSNP	rs1057518577
23andMe	rs1057518577
SNPshot	rs1057518577
SNPdbe	rs1057518577
MSV3d	rs1057518577
GWAS Ctlg	rs1057518577

Max Magnitude

0

ClinVar
Risk	rs1057518577(GT;GT)
Alt	rs1057518577(GT;GT)
Reference	Rs1057518577(TA;TA)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	GRIN2B
CLNDBN	not provided
Reversed	1
HGVS	NC_000012.11:g.13764656_13764657delTAinsAC
CLNSRC
CLNACC	RCV000414287.1,