{{Rsnum
|rsid=121909521
|Chromosome=1
|Orientation=minus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=ACTA1
|position=229433067
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=ACTA1
}}{{omim
|id=102610
|rsnum=121909521
|variant=0003
}}{{ClinVar
|rsid=121909521
|Reversed=1
|FwdREF=G
|FwdALT=C
|REF=C
|ALT=G
|RSPOS=229433067
|CHROM=1
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000a05000002110100
|GENEINFO=ACTA1:58
|GENE_NAME=ACTA1
|GENE_ID=58
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.229433067C>G
|CLNORIGIN=1
|CLNSIG=5
|Tags=RV;PM;S3D;NSM;REF;ASP;OTHERKG;LSD;OM
|CLNACC=RCV000019943.27
|CLNDBN=Myopathy, actin, congenital, with excess of thin myofilaments
|CLNDSDB=MedGen
|CLNDSDBID=C1834339
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNSRCID=NM_001100.3:c.49G>C; 102610.0003
|Disease=Myopathy
}}