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rs796052551

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs796052551(A;G)
Make rs796052551(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position9768997
GeneGRIN2A
is asnp
is mentioned by
dbSNPrs796052551
ebirs796052551
HLIrs796052551
Exacrs796052551
Varsomers796052551
Maprs796052551
PheGenIrs796052551
hapmaprs796052551
1000 genomesrs796052551
hgdprs796052551
ensemblrs796052551
gopubmedrs796052551
geneviewrs796052551
scholarrs796052551
googlers796052551
pharmgkbrs796052551
gwascentralrs796052551
openSNPrs796052551
23andMers796052551
23andMe allrs796052551
SNP Nexus

SNPshotrs796052551
SNPdbers796052551
MSV3drs796052551
GWAS Ctlgrs796052551
Max Magnitude0
ClinVar
Risk rs796052551(G;G)
Alt rs796052551(G;G)
Reference rs796052551(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene GRIN2A
CLNDBN not provided
Reversed 1
HGVS NC_000016.9:g.9862854T>C
CLNSRC
CLNACC RCV000187645.2,