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rs796052556

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796052556(C;C)
Make rs796052556(C;G)
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position9764203
GeneGRIN2A
is asnp
is mentioned by
dbSNPrs796052556
ebirs796052556
HLIrs796052556
Exacrs796052556
Varsomers796052556
Maprs796052556
PheGenIrs796052556
hapmaprs796052556
1000 genomesrs796052556
hgdprs796052556
ensemblrs796052556
gopubmedrs796052556
geneviewrs796052556
scholarrs796052556
googlers796052556
pharmgkbrs796052556
gwascentralrs796052556
openSNPrs796052556
23andMers796052556
23andMe allrs796052556
SNP Nexus

SNPshotrs796052556
SNPdbers796052556
MSV3drs796052556
GWAS Ctlgrs796052556
Max Magnitude0
ClinVar
Risk rs796052556(C;C)
Alt rs796052556(C;C)
Reference rs796052556(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene GRIN2A
CLNDBN not provided
Reversed 1
HGVS NC_000016.9:g.9858060C>G
CLNSRC
CLNACC RCV000187656.1,