{{Rsnum
|rsid=104894545
|Chromosome=17
|Orientation=minus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=ACTG1
|position=81510824
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=ACTG1
}}{{omim
|id=102560
|rsnum=104894545
|variant=0003
}}{{ClinVar
|rsid=104894545
|Reversed=1
|FwdREF=C
|FwdALT=G
|REF=G
|ALT=C
|RSPOS=79477850
|CHROM=17
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=ACTG1:71
|GENE_NAME=ACTG1
|GENE_ID=71
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000017.10:g.79477850G>C
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=102560.0003
|CLNSIG=5
|CLNCUI=C1858172
|CLNDBN=Deafness, autosomal dominant 20
|Disease=Deafness
|CLNACC=RCV000019982.26
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1434:C1858172:604717:90635
}}