{{Rsnum
|rsid=121918602
|Chromosome=1
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=RYR2
|position=237454396
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=RYR2
}}{{omim
|id=180902
|rsnum=121918602
|variant=0006
}}{{ClinVar
|rsid=121918602
|Reversed=0
|FwdREF=T
|FwdALT=C
|REF=T
|ALT=C
|RSPOS=237454396
|CHROM=1
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000a05000002110100
|GENEINFO=RYR2:6262
|GENE_NAME=RYR2
|GENE_ID=6262
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.237454396T>C
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_001035.2:c.1298T>C; 180902.0006
|CLNSIG=5
|CLNCUI=C1832931
|CLNDBN=Arrhythmogenic right ventricular cardiomyopathy, type 2
|Disease=Arrhythmogenic right ventricular cardiomyopathy
|CLNACC=RCV000013825.16
|Tags=PM;S3D;NSM;REF;ASP;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM
|CLNDSDBID=NBK1131:C1832931:600996
}}