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rs794729121

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794729121(-;-)
Make rs794729121(-;C)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position32878942
GenePKP2
is asnp
is mentioned by
dbSNPrs794729121
dbSNP (classic)rs794729121
ClinGenrs794729121
ebirs794729121
HLIrs794729121
Exacrs794729121
Gnomadrs794729121
Varsomers794729121
LitVarrs794729121
Maprs794729121
PheGenIrs794729121
Biobankrs794729121
1000 genomesrs794729121
hgdprs794729121
ensemblrs794729121
geneviewrs794729121
scholarrs794729121
googlers794729121
pharmgkbrs794729121
gwascentralrs794729121
openSNPrs794729121
23andMers794729121
SNPshotrs794729121
SNPdbers794729121
MSV3drs794729121
GWAS Ctlgrs794729121
Max Magnitude0
ClinVar
Risk rs794729121(-;-)
Alt rs794729121(-;-)
Reference Rs794729121(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene PKP2
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.33031876delG
CLNSRC
CLNACC RCV000183781.2,