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rs794729125

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(TCTAATGACA;TCTAATGACA) 0 common in clinvar
Make rs794729125(-;-)
Make rs794729125(-;TCTAATGACA)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position32841176
GenePKP2
is asnp
is mentioned by
dbSNPrs794729125
dbSNP (old)rs794729125
ClinGenrs794729125
ebirs794729125
HLIrs794729125
Exacrs794729125
Gnomadrs794729125
Varsomers794729125
Maprs794729125
PheGenIrs794729125
Biobankrs794729125
1000 genomesrs794729125
hgdprs794729125
ensemblrs794729125
gopubmedrs794729125
geneviewrs794729125
scholarrs794729125
googlers794729125
pharmgkbrs794729125
gwascentralrs794729125
openSNPrs794729125
23andMers794729125
23andMe allrs794729125
SNP Nexus

SNPshotrs794729125
SNPdbers794729125
MSV3drs794729125
GWAS Ctlgrs794729125
Max Magnitude0
ClinVar
Risk rs794729125(-;-)
Alt rs794729125(-;-)
Reference Rs794729125(TCTAATGACA;TCTAATGACA)
Significance Pathogenic
Disease not provided
Variation info
Gene PKP2
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.32994110_32994119delTGTCATTAGA
CLNSRC
CLNACC RCV000183788.1,