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rs869312868

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs869312868(A;A)
Make rs869312868(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome12
Position13571910
GeneGRIN2B
is asnp
is mentioned by
dbSNPrs869312868
ebirs869312868
HLIrs869312868
Exacrs869312868
Varsomers869312868
Maprs869312868
PheGenIrs869312868
hapmaprs869312868
1000 genomesrs869312868
hgdprs869312868
ensemblrs869312868
gopubmedrs869312868
geneviewrs869312868
scholarrs869312868
googlers869312868
pharmgkbrs869312868
gwascentralrs869312868
openSNPrs869312868
23andMers869312868
23andMe allrs869312868
SNP Nexus

SNPshotrs869312868
SNPdbers869312868
MSV3drs869312868
GWAS Ctlgrs869312868
Max Magnitude0
ClinVar
Risk rs869312868(A;A)
Alt rs869312868(A;A)
Reference rs869312868(G;G)
Significance Probable-Pathogenic
Disease Mental retardation
Variation info
Gene GRIN2B
CLNDBN Mental retardation, autosomal dominant 6
Reversed 1
HGVS NC_000012.11:g.13724844C>T
CLNSRC
CLNACC RCV000210391.1,