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rs398122825

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs398122825(C;T)
Make rs398122825(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position13611828
GeneGRIN2B
is asnp
is mentioned by
dbSNPrs398122825
ebirs398122825
HLIrs398122825
Exacrs398122825
Varsomers398122825
Maprs398122825
PheGenIrs398122825
hapmaprs398122825
1000 genomesrs398122825
hgdprs398122825
ensemblrs398122825
gopubmedrs398122825
geneviewrs398122825
scholarrs398122825
googlers398122825
pharmgkbrs398122825
gwascentralrs398122825
openSNPrs398122825
23andMers398122825
23andMe allrs398122825
SNP Nexus

SNPshotrs398122825
SNPdbers398122825
MSV3drs398122825
GWAS Ctlgrs398122825
Max Magnitude0
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,