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rs397516986

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397516986(C;T)
Make rs397516986(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position32868965
GenePKP2
is asnp
is mentioned by
dbSNPrs397516986
ebirs397516986
HLIrs397516986
Exacrs397516986
Varsomers397516986
Maprs397516986
PheGenIrs397516986
hapmaprs397516986
1000 genomesrs397516986
hgdprs397516986
ensemblrs397516986
gopubmedrs397516986
geneviewrs397516986
scholarrs397516986
googlers397516986
pharmgkbrs397516986
gwascentralrs397516986
openSNPrs397516986
23andMers397516986
23andMe allrs397516986
SNP Nexus

SNPshotrs397516986
SNPdbers397516986
MSV3drs397516986
GWAS Ctlgrs397516986
Max Magnitude0
ClinVar
Risk rs397516986(T;T)
Alt rs397516986(T;T)
Reference rs397516986(C;C)
Significance Pathogenic
Disease Arrhythmogenic right ventricular cardiomyopathy not provided Arrhythmogenic right ventricular cardiomyopathy
Variation info
Gene PKP2
CLNDBN Arrhythmogenic right ventricular cardiomyopathy, type 9 not provided Arrhythmogenic right ventricular cardiomyopathy
Reversed 1
HGVS NC_000012.11:g.33021899G>A
CLNSRC ClinVar
CLNACC RCV000038149.5, RCV000183735.2, RCV000211737.1,