Have questions? Visit https://www.reddit.com/r/SNPedia

rs796052571

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796052571(A;A)
Make rs796052571(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position13608755
GeneGRIN2B, LOC105369668
is asnp
is mentioned by
dbSNPrs796052571
ebirs796052571
HLIrs796052571
Exacrs796052571
Varsomers796052571
Maprs796052571
PheGenIrs796052571
hapmaprs796052571
1000 genomesrs796052571
hgdprs796052571
ensemblrs796052571
gopubmedrs796052571
geneviewrs796052571
scholarrs796052571
googlers796052571
pharmgkbrs796052571
gwascentralrs796052571
openSNPrs796052571
23andMers796052571
23andMe allrs796052571
SNP Nexus

SNPshotrs796052571
SNPdbers796052571
MSV3drs796052571
GWAS Ctlgrs796052571
Max Magnitude0
ClinVar
Risk rs796052571(A;A)
Alt rs796052571(A;A)
Reference rs796052571(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene GRIN2B
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.13761689C>T
CLNSRC
CLNACC RCV000187697.2,