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rs796052552

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796052552(C;T)
Make rs796052552(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position9764696
GeneGRIN2A
is asnp
is mentioned by
dbSNPrs796052552
ebirs796052552
HLIrs796052552
Exacrs796052552
Varsomers796052552
Maprs796052552
PheGenIrs796052552
hapmaprs796052552
1000 genomesrs796052552
hgdprs796052552
ensemblrs796052552
gopubmedrs796052552
geneviewrs796052552
scholarrs796052552
googlers796052552
pharmgkbrs796052552
gwascentralrs796052552
openSNPrs796052552
23andMers796052552
23andMe allrs796052552
SNP Nexus

SNPshotrs796052552
SNPdbers796052552
MSV3drs796052552
GWAS Ctlgrs796052552
Max Magnitude0
ClinVar
Risk rs796052552(T;T)
Alt rs796052552(T;T)
Reference rs796052552(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene GRIN2A
CLNDBN not provided
Reversed 1
HGVS NC_000016.9:g.9858553G>A
CLNSRC
CLNACC RCV000187646.1,