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rs876661055

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs876661055(C;C)
Make rs876661055(C;T)
ReferenceGRCh38.p2 38.2/147
Chromosome12
Position13569937
GeneGRIN2B
is asnp
is mentioned by
dbSNPrs876661055
ebirs876661055
HLIrs876661055
Exacrs876661055
Varsomers876661055
Maprs876661055
PheGenIrs876661055
hapmaprs876661055
1000 genomesrs876661055
hgdprs876661055
ensemblrs876661055
gopubmedrs876661055
geneviewrs876661055
scholarrs876661055
googlers876661055
pharmgkbrs876661055
gwascentralrs876661055
openSNPrs876661055
23andMers876661055
23andMe allrs876661055
SNP Nexus

SNPshotrs876661055
SNPdbers876661055
MSV3drs876661055
GWAS Ctlgrs876661055
Max Magnitude0
ClinVar
Risk rs876661055(C;C)
Alt rs876661055(C;C)
Reference rs876661055(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene GRIN2B
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.13722871A>G
CLNSRC
CLNACC RCV000217622.1,