{{Rsnum
|rsid=121909532
|Chromosome=1
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=ACTA1
|position=229432393
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Status=Merged
|Merged=121909522
|Gene_s=ACTA1
}}{{omim
|id=102610
|rsnum=121909532
|variant=0014
}}{{ClinVar
|rsid=121909532
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=229568140
|CHROM=1
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=050260000a15000002110100
|GENEINFO=ACTA1:58
|GENE_NAME=ACTA1
|GENE_ID=58
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.10:g.229568140C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=102610.0014
|CLNSIG=5
|CLNCUI=C1834336
|CLNDBN=Nemaline myopathy 3
|Disease=Nemaline myopathy 3
|CLNACC=SCV000040252.1
|Tags=RV;PM;S3D;NSM;REF;OTH;ASP;OTHERKG;LSD;OM
}}