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rs876657659

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs876657659(-;-)
Make rs876657659(-;C)
Make rs876657659(C;C)
ReferenceGRCh38.p2 38.2/147
Chromosome12
Position32850842
GenePKP2
is asnp
is mentioned by
dbSNPrs876657659
ebirs876657659
HLIrs876657659
Exacrs876657659
Varsomers876657659
Maprs876657659
PheGenIrs876657659
hapmaprs876657659
1000 genomesrs876657659
hgdprs876657659
ensemblrs876657659
gopubmedrs876657659
geneviewrs876657659
scholarrs876657659
googlers876657659
pharmgkbrs876657659
gwascentralrs876657659
openSNPrs876657659
23andMers876657659
23andMe allrs876657659
SNP Nexus

SNPshotrs876657659
SNPdbers876657659
MSV3drs876657659
GWAS Ctlgrs876657659
Max Magnitude0
ClinVar
Risk rs876657659(C;C)
Alt rs876657659(C;C)
Reference rs876657659(;)
Significance Probable-Pathogenic
Disease Arrhythmogenic right ventricular cardiomyopathy
Variation info
Gene PKP2
CLNDBN Arrhythmogenic right ventricular cardiomyopathy
Reversed 1
HGVS NC_000012.11:g.33003777dupG
CLNSRC
CLNACC RCV000214880.1,