{{Rsnum
|rsid=193922635
|Chromosome=1
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=ACTN2
|position=236755191
|Gene_s=ACTN2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=193922635
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=236755191
|CHROM=1
|dbSNPBuildID=136
|SSR=0
|SAO=1
|VP=0x050260000a05000002100100
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.236755191C>T
|CLNSRC=ClinVar; LabCorp
|CLNORIGIN=1
|CLNSIG=4
|CLNDBN=Cardiomyopathy; AllHighlyPenetrant
|Disease=Cardiomyopathy; AllHighlyPenetrant
|Tags=PM;S3D;NSM;REF;ASP;OTHERKG;LSD
|CLNACC=RCV000029298.1; RCV000036896.1
|CLNDSDB=MedGen:SNOMED_CT; MedGen
|CLNDSDBID=C0878544:85898001; CN169374
|GENEINFO=ACTN2:88
|GENE_ID=88
|GENE_NAME=ACTN2
|CLNSRCID=NM_001103.3:c.2147C>T; NM_001103.2:c.2147C>T
}}