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rs397517009

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397517009(-;-)
Make rs397517009(-;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position32824091
GenePKP2
is asnp
is mentioned by
dbSNPrs397517009
ebirs397517009
HLIrs397517009
Exacrs397517009
Varsomers397517009
Maprs397517009
PheGenIrs397517009
hapmaprs397517009
1000 genomesrs397517009
hgdprs397517009
ensemblrs397517009
gopubmedrs397517009
geneviewrs397517009
scholarrs397517009
googlers397517009
pharmgkbrs397517009
gwascentralrs397517009
openSNPrs397517009
23andMers397517009
23andMe allrs397517009
SNP Nexus

SNPshotrs397517009
SNPdbers397517009
MSV3drs397517009
GWAS Ctlgrs397517009
Max Magnitude0
ClinVar
Risk rs397517009(;)
Alt rs397517009(;)
Reference rs397517009(T;T)
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.32977025delA
CLNSRC ClinVar
CLNACC RCV000038186.2, RCV000183792.1,