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rs772220644

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(CG;CG) 0 common in clinvar
Make rs772220644(-;-)
Make rs772220644(-;GC)
Make rs772220644(GC;GC)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position32878042
GenePKP2
is asnp
is mentioned by
dbSNPrs772220644
dbSNP (old)rs772220644
ClinGenrs772220644
ebirs772220644
HLIrs772220644
Exacrs772220644
Gnomadrs772220644
Varsomers772220644
Maprs772220644
PheGenIrs772220644
Biobankrs772220644
1000 genomesrs772220644
hgdprs772220644
ensemblrs772220644
gopubmedrs772220644
geneviewrs772220644
scholarrs772220644
googlers772220644
pharmgkbrs772220644
gwascentralrs772220644
openSNPrs772220644
23andMers772220644
23andMe allrs772220644
SNP Nexus

SNPshotrs772220644
SNPdbers772220644
MSV3drs772220644
GWAS Ctlgrs772220644
Max Magnitude0
ClinVar
Risk rs772220644(-;-)
Alt rs772220644(-;-)
Reference Rs772220644(CG;CG)
Significance Pathogenic
Disease Arrhythmogenic right ventricular cardiomyopathy
Variation info
Gene PKP2
CLNDBN Arrhythmogenic right ventricular cardiomyopathy, type 9
Reversed 0
HGVS NC_000012.11:g.33030976_33030977delCG
CLNSRC
CLNACC RCV000464940.1,