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rs794729130

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794729130(-;-)
Make rs794729130(-;G)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position32802428
GenePKP2
is asnp
is mentioned by
dbSNPrs794729130
dbSNP (classic)rs794729130
ClinGenrs794729130
ebirs794729130
HLIrs794729130
Exacrs794729130
Gnomadrs794729130
Varsomers794729130
LitVarrs794729130
Maprs794729130
PheGenIrs794729130
Biobankrs794729130
1000 genomesrs794729130
hgdprs794729130
ensemblrs794729130
geneviewrs794729130
scholarrs794729130
googlers794729130
pharmgkbrs794729130
gwascentralrs794729130
openSNPrs794729130
23andMers794729130
SNPshotrs794729130
SNPdbers794729130
MSV3drs794729130
GWAS Ctlgrs794729130
Max Magnitude0
ClinVar
Risk rs794729130(-;-)
Alt rs794729130(-;-)
Reference Rs794729130(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PKP2
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.32955362delC
CLNSRC
CLNACC RCV000183797.2,