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rs794729124

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(TTTCATAC;TTTCATAC) 0 common in clinvar
Make rs794729124(-;-)
Make rs794729124(-;TTTCATAC)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position32868965
GenePKP2
is asnp
is mentioned by
dbSNPrs794729124
ClinGenrs794729124
ebirs794729124
HLIrs794729124
Exacrs794729124
Varsomers794729124
Maprs794729124
PheGenIrs794729124
hapmaprs794729124
1000 genomesrs794729124
hgdprs794729124
ensemblrs794729124
gopubmedrs794729124
geneviewrs794729124
scholarrs794729124
googlers794729124
pharmgkbrs794729124
gwascentralrs794729124
openSNPrs794729124
23andMers794729124
23andMe allrs794729124
SNP Nexus

SNPshotrs794729124
SNPdbers794729124
MSV3drs794729124
GWAS Ctlgrs794729124
Max Magnitude0
ClinVar
Risk rs794729124(-;-)
Alt rs794729124(-;-)
Reference Rs794729124(TTTCATAC;TTTCATAC)
Significance Pathogenic
Disease not provided Arrhythmogenic right ventricular cardiomyopathy
Variation info
Gene PKP2
CLNDBN not provided Arrhythmogenic right ventricular cardiomyopathy, type 9
Reversed 1
HGVS NC_000012.11:g.33021899_33021906delGTATGAAA
CLNSRC
CLNACC RCV000183786.1, RCV000477267.1,