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rs397516996

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397516996(-;-)
Make rs397516996(-;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position32896718
GenePKP2
is asnp
is mentioned by
dbSNPrs397516996
ebirs397516996
HLIrs397516996
Exacrs397516996
Varsomers397516996
Maprs397516996
PheGenIrs397516996
hapmaprs397516996
1000 genomesrs397516996
hgdprs397516996
ensemblrs397516996
gopubmedrs397516996
geneviewrs397516996
scholarrs397516996
googlers397516996
pharmgkbrs397516996
gwascentralrs397516996
openSNPrs397516996
23andMers397516996
23andMe allrs397516996
SNP Nexus

SNPshotrs397516996
SNPdbers397516996
MSV3drs397516996
GWAS Ctlgrs397516996
Max Magnitude0
ClinVar
Risk rs397516996(;)
Alt rs397516996(;)
Reference rs397516996(G;G)
Significance Pathogenic
Disease Arrhythmogenic right ventricular cardiomyopathy not provided
Variation info
Gene PKP2
CLNDBN Arrhythmogenic right ventricular cardiomyopathy not provided
Reversed 1
HGVS NC_000012.11:g.33049652delC
CLNSRC ClinVar
CLNACC RCV000038166.2, RCV000183791.2,