{{Rsnum
|rsid=121434420
|Chromosome=12
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=PKP2
|position=32879021
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=PKP2
}}{{omim
|id=602861
|rsnum=121434420
|variant=0001
}}{{ClinVar
|rsid=121434420
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=33031955
|CHROM=12
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=PKP2:5318
|GENE_NAME=PKP2
|GENE_ID=5318
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000012.11:g.33031955G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=602861.0001
|CLNSIG=5
|CLNCUI=C1836906
|CLNDBN=Arrhythmogenic right ventricular cardiomyopathy, type 9; Arrhythmogenic right ventricular cardiomyopathy
|Disease=Arrhythmogenic right ventricular cardiomyopathy; Arrhythmogenic right ventricular cardiomyopathy
|CLNACC=RCV000007146.1; RCV000038206.1
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM; GeneReviews:MedGen:SNOMED_CT:SNOMED_CT
|CLNDSDBID=NBK1131:C1836906:609040; NBK1131:C0349788:253528005:281170005
}}