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rs796052543

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs796052543(C;C)
Make rs796052543(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position9840781
GeneGRIN2A
is asnp
is mentioned by
dbSNPrs796052543
ebirs796052543
HLIrs796052543
Exacrs796052543
Varsomers796052543
Maprs796052543
PheGenIrs796052543
hapmaprs796052543
1000 genomesrs796052543
hgdprs796052543
ensemblrs796052543
gopubmedrs796052543
geneviewrs796052543
scholarrs796052543
googlers796052543
pharmgkbrs796052543
gwascentralrs796052543
openSNPrs796052543
23andMers796052543
23andMe allrs796052543
SNP Nexus

SNPshotrs796052543
SNPdbers796052543
MSV3drs796052543
GWAS Ctlgrs796052543
Max Magnitude0
ClinVar
Risk rs796052543(C;C)
Alt rs796052543(C;C)
Reference rs796052543(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene GRIN2A
CLNDBN not provided
Reversed 1
HGVS NC_000016.9:g.9934638A>G
CLNSRC
CLNACC RCV000187636.1,