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rs144601090

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs144601090(A;G)
Make rs144601090(G;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position32821439
GenePKP2
is asnp
is mentioned by
dbSNPrs144601090
ebirs144601090
HLIrs144601090
Exacrs144601090
Varsomers144601090
Maprs144601090
PheGenIrs144601090
hapmaprs144601090
1000 genomesrs144601090
hgdprs144601090
ensemblrs144601090
gopubmedrs144601090
geneviewrs144601090
scholarrs144601090
googlers144601090
pharmgkbrs144601090
gwascentralrs144601090
openSNPrs144601090
23andMers144601090
23andMe allrs144601090
SNP Nexus

SNPshotrs144601090
SNPdbers144601090
MSV3drs144601090
GWAS Ctlgrs144601090
Max Magnitude0
ClinVar
Risk rs144601090(G;G)
Alt rs144601090(G;G)
Reference rs144601090(A;A)
Significance Other
Disease Arrhythmogenic right ventricular cardiomyopathy not specified
Variation info
Gene PKP2
CLNDBN Arrhythmogenic right ventricular cardiomyopathy not specified
Reversed 0
HGVS NC_000012.11:g.32974373A>G
CLNSRC ClinVar University of Washington
CLNACC RCV000038195.3, RCV000154180.2,