{{Rsnum
|rsid=121909530
|Chromosome=1
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=ACTA1
|position=229432134
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=ACTA1
}}{{omim
|id=102610
|rsnum=121909530
|variant=0012
}}{{ClinVar
|rsid=121909530
|Reversed=1
|FwdREF=T
|FwdALT=C
|REF=A
|ALT=G
|RSPOS=229432134
|CHROM=1
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050368000a05000002110100
|GENEINFO=ACTA1:58
|GENE_NAME=ACTA1
|GENE_ID=58
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.229432134A>G
|CLNSRC=ClinVar; GeneReviews; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_001100.3:c.668T>C; NBK1259; 102610.0012
|CLNSIG=5
|CLNCUI=C0546264
|CLNDBN=Congenital myopathy with fiber type disproportion
|Disease=Congenital myopathy with fiber type disproportion
|CLNACC=RCV000019952.27
|Tags=RV;PM;PMC;S3D;SLO;NSM;REF;ASP;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1259:C0546264:255310:ORPHA2020:240084007
}}{{PMID Auto
|PMID=15468086
|Title=Actin mutations are one cause of congenital fibre type disproportion.
}}