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rs796052570

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs796052570(A;G)
Make rs796052570(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position13753879
GeneGRIN2B
is asnp
is mentioned by
dbSNPrs796052570
ebirs796052570
HLIrs796052570
Exacrs796052570
Varsomers796052570
Maprs796052570
PheGenIrs796052570
hapmaprs796052570
1000 genomesrs796052570
hgdprs796052570
ensemblrs796052570
gopubmedrs796052570
geneviewrs796052570
scholarrs796052570
googlers796052570
pharmgkbrs796052570
gwascentralrs796052570
openSNPrs796052570
23andMers796052570
23andMe allrs796052570
SNP Nexus

SNPshotrs796052570
SNPdbers796052570
MSV3drs796052570
GWAS Ctlgrs796052570
Max Magnitude0
ClinVar
Risk rs796052570(G;G)
Alt rs796052570(G;G)
Reference rs796052570(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene GRIN2B
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.13906813T>C
CLNSRC
CLNACC RCV000187696.1,