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rs796052583

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796052583(C;T)
Make rs796052583(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position13608706
GeneGRIN2B, LOC105369668
is asnp
is mentioned by
dbSNPrs796052583
ebirs796052583
HLIrs796052583
Exacrs796052583
Varsomers796052583
Maprs796052583
PheGenIrs796052583
hapmaprs796052583
1000 genomesrs796052583
hgdprs796052583
ensemblrs796052583
gopubmedrs796052583
geneviewrs796052583
scholarrs796052583
googlers796052583
pharmgkbrs796052583
gwascentralrs796052583
openSNPrs796052583
23andMers796052583
23andMe allrs796052583
SNP Nexus

SNPshotrs796052583
SNPdbers796052583
MSV3drs796052583
GWAS Ctlgrs796052583
Max Magnitude0
ClinVar
Risk rs796052583(T;T)
Alt rs796052583(T;T)
Reference rs796052583(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene GRIN2B
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.13761640G>A
CLNSRC
CLNACC RCV000187719.1,