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rs794729127

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;T) 6.7 Arrhythmogenic right ventricular dysplasia
(T;T) 0 common in clinvar


Make rs794729127(-;-)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position32841052
GenePKP2
is asnp
is mentioned by
dbSNPrs794729127
dbSNP (classic)rs794729127
ClinGenrs794729127
ebirs794729127
HLIrs794729127
Exacrs794729127
Gnomadrs794729127
Varsomers794729127
LitVarrs794729127
Maprs794729127
PheGenIrs794729127
Biobankrs794729127
1000 genomesrs794729127
hgdprs794729127
ensemblrs794729127
geneviewrs794729127
scholarrs794729127
googlers794729127
pharmgkbrs794729127
gwascentralrs794729127
openSNPrs794729127
23andMers794729127
SNPshotrs794729127
SNPdbers794729127
MSV3drs794729127
GWAS Ctlgrs794729127
Max Magnitude6.7
ClinVar
Risk rs794729127(-;-)
Alt rs794729127(-;-)
Reference Rs794729127(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene PKP2
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.32993986delA
CLNSRC
CLNACC RCV000183790.2,