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rs796052547

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs796052547(A;G)
Make rs796052547(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position9822382
GeneGRIN2A
is asnp
is mentioned by
dbSNPrs796052547
ebirs796052547
HLIrs796052547
Exacrs796052547
Varsomers796052547
Maprs796052547
PheGenIrs796052547
hapmaprs796052547
1000 genomesrs796052547
hgdprs796052547
ensemblrs796052547
gopubmedrs796052547
geneviewrs796052547
scholarrs796052547
googlers796052547
pharmgkbrs796052547
gwascentralrs796052547
openSNPrs796052547
23andMers796052547
23andMe allrs796052547
SNP Nexus

SNPshotrs796052547
SNPdbers796052547
MSV3drs796052547
GWAS Ctlgrs796052547
Max Magnitude0
ClinVar
Risk rs796052547(G;G)
Alt rs796052547(G;G)
Reference rs796052547(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene GRIN2A
CLNDBN not provided
Reversed 1
HGVS NC_000016.9:g.9916239T>C
CLNSRC
CLNACC RCV000187640.2,