{{Rsnum
|rsid=398122936
|Chromosome=1
|Orientation=minus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=ACTA1
|position=229431727
|Gene_s=ACTA1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=G
|CHROM=1
|CLNACC=RCV000043506.27
|CLNALLE=1
|CLNDBN=Nemaline myopathy 3
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1288:C1834336:161800:ORPHA607
|CLNHGVS=NC_000001.11:g.229431727C>G
|CLNSIG=5
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNSRCID=NM_001100.3:c.984G>C; 102610.0016
|Disease=Nemaline myopathy 3
|FwdALT=C
|FwdREF=G
|GENEINFO=ACTA1:58
|GENE_ID=58
|GENE_NAME=ACTA1
|REF=C
|RSPOS=229431727
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;NSM;REF;ASP;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000a05000002110100
|WGT=1
|dbSNPBuildID=138
|rsid=398122936
|CLNORIGIN=1
}}