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rs876661151

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876661151(G;T)
Make rs876661151(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome12
Position13608611
GeneGRIN2B, LOC105369668
is asnp
is mentioned by
dbSNPrs876661151
ebirs876661151
HLIrs876661151
Exacrs876661151
Varsomers876661151
Maprs876661151
PheGenIrs876661151
hapmaprs876661151
1000 genomesrs876661151
hgdprs876661151
ensemblrs876661151
gopubmedrs876661151
geneviewrs876661151
scholarrs876661151
googlers876661151
pharmgkbrs876661151
gwascentralrs876661151
openSNPrs876661151
23andMers876661151
23andMe allrs876661151
SNP Nexus

SNPshotrs876661151
SNPdbers876661151
MSV3drs876661151
GWAS Ctlgrs876661151
Max Magnitude0
ClinVar
Risk rs876661151(T;T)
Alt rs876661151(T;T)
Reference rs876661151(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene GRIN2B
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.13761545C>A
CLNSRC
CLNACC RCV000221616.1,