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rs794729116

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794729116(A;A)
Make rs794729116(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position32802402
GenePKP2
is asnp
is mentioned by
dbSNPrs794729116
ebirs794729116
HLIrs794729116
Exacrs794729116
Varsomers794729116
Maprs794729116
PheGenIrs794729116
hapmaprs794729116
1000 genomesrs794729116
hgdprs794729116
ensemblrs794729116
gopubmedrs794729116
geneviewrs794729116
scholarrs794729116
googlers794729116
pharmgkbrs794729116
gwascentralrs794729116
openSNPrs794729116
23andMers794729116
23andMe allrs794729116
SNP Nexus

SNPshotrs794729116
SNPdbers794729116
MSV3drs794729116
GWAS Ctlgrs794729116
Max Magnitude0
ClinVar
Risk rs794729116(A,T;A,T)
Alt rs794729116(A,T;A,T)
Reference rs794729116(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene PKP2
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.32955336C>A; NC_000012.11:g.32955336C>T
CLNSRC
CLNACC RCV000183775.1, RCV000183774.2,