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rs397517015

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397517015(G;T)
Make rs397517015(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position32821502
GenePKP2
is asnp
is mentioned by
dbSNPrs397517015
ebirs397517015
HLIrs397517015
Exacrs397517015
Varsomers397517015
Maprs397517015
PheGenIrs397517015
hapmaprs397517015
1000 genomesrs397517015
hgdprs397517015
ensemblrs397517015
gopubmedrs397517015
geneviewrs397517015
scholarrs397517015
googlers397517015
pharmgkbrs397517015
gwascentralrs397517015
openSNPrs397517015
23andMers397517015
23andMe allrs397517015
SNP Nexus

SNPshotrs397517015
SNPdbers397517015
MSV3drs397517015
GWAS Ctlgrs397517015
Max Magnitude0
ClinVar
Risk rs397517015(T;T)
Alt rs397517015(T;T)
Reference rs397517015(G;G)
Significance Pathogenic
Disease Arrhythmogenic right ventricular cardiomyopathy
Variation info
Gene PKP2
CLNDBN Arrhythmogenic right ventricular cardiomyopathy
Reversed 1
HGVS NC_000012.11:g.32974436C>A
CLNSRC ClinVar
CLNACC RCV000038194.2,