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

rs372827156

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs372827156(A;A)
Make rs372827156(A;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position32850907
GenePKP2
is asnp
is mentioned by
dbSNPrs372827156
ebirs372827156
HLIrs372827156
Exacrs372827156
Varsomers372827156
Maprs372827156
PheGenIrs372827156
hapmaprs372827156
1000 genomesrs372827156
hgdprs372827156
ensemblrs372827156
gopubmedrs372827156
geneviewrs372827156
scholarrs372827156
googlers372827156
pharmgkbrs372827156
gwascentralrs372827156
openSNPrs372827156
23andMers372827156
23andMe allrs372827156
SNP Nexus

SNPshotrs372827156
SNPdbers372827156
MSV3drs372827156
GWAS Ctlgrs372827156
Max Magnitude0
ClinVar
Risk rs372827156(A;A)
Alt rs372827156(A;A)
Reference rs372827156(G;G)
Significance Other
Disease Arrhythmogenic right ventricular cardiomyopathy Arrhythmogenic right ventricular cardiomyopathy not provided
Variation info
Gene PKP2
CLNDBN Arrhythmogenic right ventricular cardiomyopathy Arrhythmogenic right ventricular cardiomyopathy, type 9 not provided
Reversed 0
HGVS NC_000012.11:g.33003841G>A
CLNSRC ClinVar University of Washington
CLNACC RCV000038155.3, RCV000154178.3, RCV000183740.2,