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rs786204393

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs786204393(C;T)
Make rs786204393(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position32850967
GenePKP2
is asnp
is mentioned by
dbSNPrs786204393
ebirs786204393
HLIrs786204393
Exacrs786204393
Varsomers786204393
Maprs786204393
PheGenIrs786204393
hapmaprs786204393
1000 genomesrs786204393
hgdprs786204393
ensemblrs786204393
gopubmedrs786204393
geneviewrs786204393
scholarrs786204393
googlers786204393
pharmgkbrs786204393
gwascentralrs786204393
openSNPrs786204393
23andMers786204393
23andMe allrs786204393
SNP Nexus

SNPshotrs786204393
SNPdbers786204393
MSV3drs786204393
GWAS Ctlgrs786204393
Max Magnitude0
ClinVar
Risk rs786204393(T;T)
Alt rs786204393(T;T)
Reference rs786204393(C;C)
Significance Probable-Pathogenic
Disease Arrhythmogenic right ventricular cardiomyopathy
Variation info
Gene PKP2
CLNDBN Arrhythmogenic right ventricular cardiomyopathy, type 9
Reversed 1
HGVS NC_000012.11:g.33003901G>A
CLNSRC
CLNACC RCV000168933.1,