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rs796052545

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs796052545(A;G)
Make rs796052545(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position9829487
GeneGRIN2A
is asnp
is mentioned by
dbSNPrs796052545
ebirs796052545
HLIrs796052545
Exacrs796052545
Varsomers796052545
Maprs796052545
PheGenIrs796052545
hapmaprs796052545
1000 genomesrs796052545
hgdprs796052545
ensemblrs796052545
gopubmedrs796052545
geneviewrs796052545
scholarrs796052545
googlers796052545
pharmgkbrs796052545
gwascentralrs796052545
openSNPrs796052545
23andMers796052545
23andMe allrs796052545
SNP Nexus

SNPshotrs796052545
SNPdbers796052545
MSV3drs796052545
GWAS Ctlgrs796052545
Max Magnitude0
ClinVar
Risk rs796052545(G;G)
Alt rs796052545(G;G)
Reference rs796052545(A;A)
Significance Probable-Pathogenic
Disease not specified
Variation info
Gene GRIN2A
CLNDBN not specified
Reversed 1
HGVS NC_000016.9:g.9923344T>C
CLNSRC
CLNACC RCV000187638.2,