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rs397517003

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397517003(A;A)
Make rs397517003(A;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position32841027
GenePKP2
is asnp
is mentioned by
dbSNPrs397517003
ebirs397517003
HLIrs397517003
Exacrs397517003
Varsomers397517003
Maprs397517003
PheGenIrs397517003
hapmaprs397517003
1000 genomesrs397517003
hgdprs397517003
ensemblrs397517003
gopubmedrs397517003
geneviewrs397517003
scholarrs397517003
googlers397517003
pharmgkbrs397517003
gwascentralrs397517003
openSNPrs397517003
23andMers397517003
23andMe allrs397517003
SNP Nexus

SNPshotrs397517003
SNPdbers397517003
MSV3drs397517003
GWAS Ctlgrs397517003
Max Magnitude0
ClinVar
Risk rs397517003(A;A)
Alt rs397517003(A;A)
Reference rs397517003(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.32993961C>T
CLNSRC ClinVar
CLNACC RCV000038177.2, RCV000183750.2,