rs1057519612

Orientation

minus

Stabilized

minus

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

Make rs1057519612(A;G)

Make rs1057519612(G;G)

Reference

GRCh38.p7 38.3/150

Chromosome

12

Position

13567265

Gene

GRIN2B

is a	snp
is	mentioned by
dbSNP	rs1057519612
dbSNP (classic)	rs1057519612
ClinGen	rs1057519612
ebi	rs1057519612
HLI	rs1057519612
Exac	rs1057519612
Gnomad	rs1057519612
Varsome	rs1057519612
LitVar	rs1057519612
Map	rs1057519612
PheGenI	rs1057519612
Biobank	rs1057519612
1000 genomes	rs1057519612
hgdp	rs1057519612
ensembl	rs1057519612
geneview	rs1057519612
scholar	rs1057519612
google	rs1057519612
pharmgkb	rs1057519612
gwascentral	rs1057519612
openSNP	rs1057519612
23andMe	rs1057519612
SNPshot	rs1057519612
SNPdbe	rs1057519612
MSV3d	rs1057519612
GWAS Ctlg	rs1057519612

Max Magnitude

0

ClinVar
Risk	rs1057519612(G;G)
Alt	rs1057519612(G;G)
Reference	Rs1057519612(A;A)
Significance	Pathogenic
Disease	Mental retardation
Variation	info
Gene	GRIN2B
CLNDBN	Mental retardation, autosomal dominant 6
Reversed	1
HGVS	NC_000012.11:g.13720199T>C
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000022583.27,