{{Rsnum
|rsid=267606626
|Chromosome=1
|Orientation=minus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=ACTA1
|position=229432788
|Gene_s=ACTA1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=A
|CHROM=1
|CLNACC=RCV000019955.27
|CLNALLE=1
|CLNDBN=Nemaline myopathy 3
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1288:C1834336:161800:ORPHA607
|CLNHGVS=NC_000001.11:g.229432788C>A
|CLNSIG=5
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNSRCID=NM_001100.3:c.222G>T; 102610.0015
|Disease=Nemaline myopathy 3
|FwdALT=T
|FwdREF=G
|GENEINFO=ACTA1:58
|GENE_ID=58
|GENE_NAME=ACTA1
|REF=C
|RSPOS=229432788
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;S3D;NSM;REF;ASP;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050260000a05000002110100
|WGT=1
|dbSNPBuildID=137
|rsid=267606626
|CLNORIGIN=1
}}