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rs876661076

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs876661076(A;C)
Make rs876661076(C;C)
ReferenceGRCh38.p2 38.2/147
Chromosome12
Position13567171
GeneGRIN2B
is asnp
is mentioned by
dbSNPrs876661076
ebirs876661076
HLIrs876661076
Exacrs876661076
Varsomers876661076
Maprs876661076
PheGenIrs876661076
hapmaprs876661076
1000 genomesrs876661076
hgdprs876661076
ensemblrs876661076
gopubmedrs876661076
geneviewrs876661076
scholarrs876661076
googlers876661076
pharmgkbrs876661076
gwascentralrs876661076
openSNPrs876661076
23andMers876661076
23andMe allrs876661076
SNP Nexus

SNPshotrs876661076
SNPdbers876661076
MSV3drs876661076
GWAS Ctlgrs876661076
Max Magnitude0
ClinVar
Risk rs876661076(C;C)
Alt rs876661076(C;C)
Reference rs876661076(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene GRIN2B
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.13720105T>G
CLNSRC
CLNACC RCV000214028.1,