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

rs786204389

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs786204389(A;T)
Make rs786204389(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position32878545
GenePKP2
is asnp
is mentioned by
dbSNPrs786204389
ebirs786204389
HLIrs786204389
Exacrs786204389
Varsomers786204389
Maprs786204389
PheGenIrs786204389
hapmaprs786204389
1000 genomesrs786204389
hgdprs786204389
ensemblrs786204389
gopubmedrs786204389
geneviewrs786204389
scholarrs786204389
googlers786204389
pharmgkbrs786204389
gwascentralrs786204389
openSNPrs786204389
23andMers786204389
23andMe allrs786204389
SNP Nexus

SNPshotrs786204389
SNPdbers786204389
MSV3drs786204389
GWAS Ctlgrs786204389
Max Magnitude0
ClinVar
Risk rs786204389(T;T)
Alt rs786204389(T;T)
Reference rs786204389(A;A)
Significance Pathogenic
Disease Arrhythmogenic right ventricular cardiomyopathy not provided
Variation info
Gene PKP2
CLNDBN Arrhythmogenic right ventricular cardiomyopathy, type 9 not provided
Reversed 1
HGVS NC_000012.11:g.33031479T>A
CLNSRC
CLNACC RCV000168929.1, RCV000183723.2,