rs398122825

Orientation

plus

Stabilized

plus

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

Make rs398122825(C;T)

Make rs398122825(T;T)

Reference

GRCh38 38.1/141

Chromosome

12

Position

13611828

Gene	GRIN2B, LOC105369668

is a	snp
is	mentioned by
dbSNP	rs398122825
dbSNP (classic)	rs398122825
ClinGen	rs398122825
ebi	rs398122825
HLI	rs398122825
Exac	rs398122825
Gnomad	rs398122825
Varsome	rs398122825
LitVar	rs398122825
Map	rs398122825
PheGenI	rs398122825
Biobank	rs398122825
1000 genomes	rs398122825
hgdp	rs398122825
ensembl	rs398122825
geneview	rs398122825
scholar	rs398122825
google	rs398122825
pharmgkb	rs398122825
gwascentral	rs398122825
openSNP	rs398122825
23andMe	rs398122825
SNPshot	rs398122825
SNPdbe	rs398122825
MSV3d	rs398122825
GWAS Ctlg	rs398122825

Max Magnitude

0

ClinVar
Risk	rs398122825(T;T)
Alt	rs398122825(T;T)
Reference	Rs398122825(C;C)
Significance	Pathogenic
Disease	Mental retardation
Variation	info
Gene	GRIN2B
CLNDBN	Mental retardation, autosomal dominant 6
Reversed	0
HGVS	NC_000012.11:g.13764762C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000032864.27,