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rs727504786

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs727504786(-;-)
Make rs727504786(-;A)
ReferenceGRCh38.p2 38.2/144
Chromosome12
Position32792670
GenePKP2
is asnp
is mentioned by
dbSNPrs727504786
ebirs727504786
HLIrs727504786
Exacrs727504786
Varsomers727504786
Maprs727504786
PheGenIrs727504786
hapmaprs727504786
1000 genomesrs727504786
hgdprs727504786
ensemblrs727504786
gopubmedrs727504786
geneviewrs727504786
scholarrs727504786
googlers727504786
pharmgkbrs727504786
gwascentralrs727504786
openSNPrs727504786
23andMers727504786
23andMe allrs727504786
SNP Nexus

SNPshotrs727504786
SNPdbers727504786
MSV3drs727504786
GWAS Ctlgrs727504786
Max Magnitude0
ClinVar
Risk rs727504786(;)
Alt rs727504786(;)
Reference rs727504786(A;A)
Significance Probable-Pathogenic
Disease Arrhythmogenic right ventricular cardiomyopathy
Variation info
Gene PKP2
CLNDBN Arrhythmogenic right ventricular cardiomyopathy
Reversed 1
HGVS NC_000012.11:g.32945604delT
CLNSRC
CLNACC RCV000156104.2,