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rs794729120

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs794729120(-;T)
Make rs794729120(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position32878999
GenePKP2
is asnp
is mentioned by
dbSNPrs794729120
dbSNP (old)rs794729120
ClinGenrs794729120
ebirs794729120
HLIrs794729120
Exacrs794729120
Gnomadrs794729120
Varsomers794729120
Maprs794729120
PheGenIrs794729120
Biobankrs794729120
1000 genomesrs794729120
hgdprs794729120
ensemblrs794729120
gopubmedrs794729120
geneviewrs794729120
scholarrs794729120
googlers794729120
pharmgkbrs794729120
gwascentralrs794729120
openSNPrs794729120
23andMers794729120
23andMe allrs794729120
SNP Nexus

SNPshotrs794729120
SNPdbers794729120
MSV3drs794729120
GWAS Ctlgrs794729120
Max Magnitude0
ClinVar
Risk rs794729120(T;T)
Alt rs794729120(T;T)
Reference Rs794729120(-;-)
Significance Pathogenic
Disease not provided
Variation info
Gene PKP2
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.33031934dupA
CLNSRC
CLNACC RCV000183780.1,