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rs796052572

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796052572(C;T)
Make rs796052572(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position13571915
GeneGRIN2B
is asnp
is mentioned by
dbSNPrs796052572
ebirs796052572
HLIrs796052572
Exacrs796052572
Varsomers796052572
Maprs796052572
PheGenIrs796052572
hapmaprs796052572
1000 genomesrs796052572
hgdprs796052572
ensemblrs796052572
gopubmedrs796052572
geneviewrs796052572
scholarrs796052572
googlers796052572
pharmgkbrs796052572
gwascentralrs796052572
openSNPrs796052572
23andMers796052572
23andMe allrs796052572
SNP Nexus

SNPshotrs796052572
SNPdbers796052572
MSV3drs796052572
GWAS Ctlgrs796052572
Max Magnitude0
ClinVar
Risk rs796052572(T;T)
Alt rs796052572(T;T)
Reference rs796052572(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene GRIN2B
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.13724849G>A
CLNSRC
CLNACC RCV000187698.1,