{{Rsnum
|rsid=121434525
|Gene=ACTN2
|Chromosome=1
|position=236686699
|Orientation=plus
|GMAF=0.0009183
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=ACTN2
}}{{omim
|id=102573
|rsnum=121434525
|variant=0001
}}{{ClinVar
|rsid=121434525
|Reversed=0
|FwdREF=A
|FwdALT=G
|REF=A
|ALT=G
|RSPOS=236686699
|CHROM=1
|GMAF=0.0009
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050060400a05040016110100
|GENEINFO=ACTN2:88
|GENE_NAME=ACTN2
|GENE_ID=88
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.236686699A>G
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_001103.3:c.26A>G; NM_001278344.1:c.-796A>G; 102573.0001
|CLNSIG=5
|CLNCUI=C2677338
|CLNDBN=Dilated cardiomyopathy 1AA; AllHighlyPenetrant
|Disease=Dilated cardiomyopathy 1AA; AllHighlyPenetrant
|CLNACC=RCV000019977.27; RCV000036908.1
|Tags=PM;NSM;REF;U5;ASP;VLD;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=0.9991; 0.0009183
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet; MedGen
|CLNDSDBID=NBK1309:C2677338:612158:ORPHA154; CN169374
|COMMON=0
}}