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rs794729118

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794729118(-;-)
Make rs794729118(-;C)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position32796213
GenePKP2
is asnp
is mentioned by
dbSNPrs794729118
dbSNP (classic)rs794729118
ClinGenrs794729118
ebirs794729118
HLIrs794729118
Exacrs794729118
Gnomadrs794729118
Varsomers794729118
LitVarrs794729118
Maprs794729118
PheGenIrs794729118
Biobankrs794729118
1000 genomesrs794729118
hgdprs794729118
ensemblrs794729118
geneviewrs794729118
scholarrs794729118
googlers794729118
pharmgkbrs794729118
gwascentralrs794729118
openSNPrs794729118
23andMers794729118
SNPshotrs794729118
SNPdbers794729118
MSV3drs794729118
GWAS Ctlgrs794729118
Max Magnitude0
ClinVar
Risk rs794729118(-;-)
Alt rs794729118(-;-)
Reference Rs794729118(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene PKP2
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.32949147delG
CLNSRC
CLNACC RCV000183777.1,