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rs397517008

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397517008(-;-)
Make rs397517008(-;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position32824092
GenePKP2
is asnp
is mentioned by
dbSNPrs397517008
ebirs397517008
HLIrs397517008
Exacrs397517008
Varsomers397517008
Maprs397517008
PheGenIrs397517008
hapmaprs397517008
1000 genomesrs397517008
hgdprs397517008
ensemblrs397517008
gopubmedrs397517008
geneviewrs397517008
scholarrs397517008
googlers397517008
pharmgkbrs397517008
gwascentralrs397517008
openSNPrs397517008
23andMers397517008
23andMe allrs397517008
SNP Nexus

SNPshotrs397517008
SNPdbers397517008
MSV3drs397517008
GWAS Ctlgrs397517008
Max Magnitude0
ClinVar
Risk
Alt
Reference Rs397517008(G;G)
Significance Probable-Pathogenic
Disease Arrhythmogenic right ventricular cardiomyopathy
Variation info
Gene PKP2
CLNDBN Arrhythmogenic right ventricular cardiomyopathy
Reversed 1
HGVS NC_000012.11:g.32977026delC
CLNSRC ClinVar
CLNACC RCV000038185.2,