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rs876661219

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs876661219(C;C)
Make rs876661219(C;T)
ReferenceGRCh38.p2 38.2/147
Chromosome12
Position13571891
GeneGRIN2B
is asnp
is mentioned by
dbSNPrs876661219
ClinGenrs876661219
ebirs876661219
HLIrs876661219
Exacrs876661219
Varsomers876661219
Maprs876661219
PheGenIrs876661219
hapmaprs876661219
1000 genomesrs876661219
hgdprs876661219
ensemblrs876661219
gopubmedrs876661219
geneviewrs876661219
scholarrs876661219
googlers876661219
pharmgkbrs876661219
gwascentralrs876661219
openSNPrs876661219
23andMers876661219
23andMe allrs876661219
SNP Nexus

SNPshotrs876661219
SNPdbers876661219
MSV3drs876661219
GWAS Ctlgrs876661219
Max Magnitude0
ClinVar
Risk rs876661219(C;C)
Alt rs876661219(C;C)
Reference Rs876661219(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene GRIN2B
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.13724825A>G
CLNSRC
CLNACC RCV000214460.1,