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rs794729126

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794729126(-;-)
Make rs794729126(-;C)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position32841137
GenePKP2
is asnp
is mentioned by
dbSNPrs794729126
dbSNP (classic)rs794729126
ClinGenrs794729126
ebirs794729126
HLIrs794729126
Exacrs794729126
Gnomadrs794729126
Varsomers794729126
LitVarrs794729126
Maprs794729126
PheGenIrs794729126
Biobankrs794729126
1000 genomesrs794729126
hgdprs794729126
ensemblrs794729126
geneviewrs794729126
scholarrs794729126
googlers794729126
pharmgkbrs794729126
gwascentralrs794729126
openSNPrs794729126
23andMers794729126
SNPshotrs794729126
SNPdbers794729126
MSV3drs794729126
GWAS Ctlgrs794729126
Max Magnitude0
ClinVar
Risk rs794729126(-;-)
Alt rs794729126(-;-)
Reference Rs794729126(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene PKP2
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.32994071delG
CLNSRC
CLNACC RCV000183789.2,