{{Rsnum
|rsid=121912676
|Chromosome=15
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=ACTC1
|position=34793431
|Gene_s=ACTC1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=102540
|rsnum=121912676
|variant=0004
}}{{ClinVar
|rsid=121912676
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=35085632
|CHROM=15
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=ACTC1:70
|GENE_NAME=ACTC1
|GENE_ID=70
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000015.9:g.35085632G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=102540.0004
|CLNSIG=5
|CLNCUI=C2677506
|CLNDBN=Familial hypertrophic cardiomyopathy 11; AllHighlyPenetrant
|Disease=Familial hypertrophic cardiomyopathy 11; AllHighlyPenetrant
|CLNACC=RCV000019991.26; RCV000038323.1
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM; MedGen
|CLNDSDBID=NBK1768:C2677506:612098; CN169374
}}