{{Rsnum
|rsid=121909525
|Chromosome=1
|Orientation=minus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=ACTA1
|position=229431994
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=ACTA1
}}{{omim
|id=102610
|rsnum=121909525
|variant=0007
}}{{ClinVar
|rsid=121909525
|Reversed=1
|FwdREF=G
|FwdALT=T
|REF=C
|ALT=A
|RSPOS=229431994
|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.229431994C>A
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_001100.3:c.808G>T; 102610.0007
|CLNSIG=5
|CLNCUI=C1834336
|CLNDBN=Nemaline myopathy 3
|Disease=Nemaline myopathy 3
|CLNACC=RCV000019947.27
|Tags=RV;PM;S3D;NSM;REF;ASP;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1288:C1834336:161800:ORPHA607
}}