Have questions? Visit https://www.reddit.com/r/SNPedia

rs397516994

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397516994(C;C)
Make rs397516994(C;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position32850765
GenePKP2
is asnp
is mentioned by
dbSNPrs397516994
ebirs397516994
HLIrs397516994
Exacrs397516994
Varsomers397516994
Maprs397516994
PheGenIrs397516994
hapmaprs397516994
1000 genomesrs397516994
hgdprs397516994
ensemblrs397516994
gopubmedrs397516994
geneviewrs397516994
scholarrs397516994
googlers397516994
pharmgkbrs397516994
gwascentralrs397516994
openSNPrs397516994
23andMers397516994
23andMe allrs397516994
SNP Nexus

SNPshotrs397516994
SNPdbers397516994
MSV3drs397516994
GWAS Ctlgrs397516994
Max Magnitude0
ClinVar
Risk rs397516994(C;C)
Alt rs397516994(C;C)
Reference rs397516994(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.33003699C>G
CLNSRC ClinVar
CLNACC RCV000038161.4, RCV000183806.2,