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rs796052563

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796052563(A;A)
Make rs796052563(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position9822348
GeneGRIN2A
is asnp
is mentioned by
dbSNPrs796052563
ebirs796052563
HLIrs796052563
Exacrs796052563
Varsomers796052563
Maprs796052563
PheGenIrs796052563
hapmaprs796052563
1000 genomesrs796052563
hgdprs796052563
ensemblrs796052563
gopubmedrs796052563
geneviewrs796052563
scholarrs796052563
googlers796052563
pharmgkbrs796052563
gwascentralrs796052563
openSNPrs796052563
23andMers796052563
23andMe allrs796052563
SNP Nexus

SNPshotrs796052563
SNPdbers796052563
MSV3drs796052563
GWAS Ctlgrs796052563
Max Magnitude0
ClinVar
Risk rs796052563(A;A)
Alt rs796052563(A;A)
Reference rs796052563(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene GRIN2A
CLNDBN not provided
Reversed 1
HGVS NC_000016.9:g.9916205C>T
CLNSRC
CLNACC RCV000187676.1,