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rs876661064

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs876661064(C;T)
Make rs876661064(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome12
Position13569988
GeneGRIN2B
is asnp
is mentioned by
dbSNPrs876661064
ebirs876661064
HLIrs876661064
Exacrs876661064
Varsomers876661064
Maprs876661064
PheGenIrs876661064
hapmaprs876661064
1000 genomesrs876661064
hgdprs876661064
ensemblrs876661064
gopubmedrs876661064
geneviewrs876661064
scholarrs876661064
googlers876661064
pharmgkbrs876661064
gwascentralrs876661064
openSNPrs876661064
23andMers876661064
23andMe allrs876661064
SNP Nexus

SNPshotrs876661064
SNPdbers876661064
MSV3drs876661064
GWAS Ctlgrs876661064
Max Magnitude0
ClinVar
Risk rs876661064(T;T)
Alt rs876661064(T;T)
Reference rs876661064(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene GRIN2B
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.13722922G>A
CLNSRC
CLNACC RCV000222391.1,